Matches in Nanopublications for { ?s ?p "[The secondary ?-dystroglycanopathies usually present in infancy as congenital muscular dystrophies but may manifest later in childhood or adult life (limb-girdle muscular dystrophy (LGMD) 2I, LGMD2K, LGMD2M, LGMD2N, and LGMD2O).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP914938.RAA8VFahOHqbrQZNHrNJdttC-5g13fMeyKHYpC01-FSNo130_assertion description "[The secondary ?-dystroglycanopathies usually present in infancy as congenital muscular dystrophies but may manifest later in childhood or adult life (limb-girdle muscular dystrophy (LGMD) 2I, LGMD2K, LGMD2M, LGMD2N, and LGMD2O).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP914938.RAA8VFahOHqbrQZNHrNJdttC-5g13fMeyKHYpC01-FSNo130_provenance.
- NP920771.RAsarER2mGnmP0TFy-BWaFtTZI449-6hn7-t1i9VCGDh8130_assertion description "[The secondary ?-dystroglycanopathies usually present in infancy as congenital muscular dystrophies but may manifest later in childhood or adult life (limb-girdle muscular dystrophy (LGMD) 2I, LGMD2K, LGMD2M, LGMD2N, and LGMD2O).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP920771.RAsarER2mGnmP0TFy-BWaFtTZI449-6hn7-t1i9VCGDh8130_provenance.
- NP662132.RAp6_OQrwLtEnGqQKxUtftZef2JKa16TNkeLoTm2VEASk130_assertion description "[The secondary ?-dystroglycanopathies usually present in infancy as congenital muscular dystrophies but may manifest later in childhood or adult life (limb-girdle muscular dystrophy (LGMD) 2I, LGMD2K, LGMD2M, LGMD2N, and LGMD2O).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP662132.RAp6_OQrwLtEnGqQKxUtftZef2JKa16TNkeLoTm2VEASk130_provenance.
- NP863399.RASiFpNAVuSbckdiAB7ReaB7tEgSTr7sXDwTd7V_txPns130_assertion description "[The secondary ?-dystroglycanopathies usually present in infancy as congenital muscular dystrophies but may manifest later in childhood or adult life (limb-girdle muscular dystrophy (LGMD) 2I, LGMD2K, LGMD2M, LGMD2N, and LGMD2O).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP863399.RASiFpNAVuSbckdiAB7ReaB7tEgSTr7sXDwTd7V_txPns130_provenance.
- NP863668.RAbl6aU_2z_3qLaNtB4mpNiQgfmNndalG45GdTgY0ZEfI130_assertion description "[The secondary ?-dystroglycanopathies usually present in infancy as congenital muscular dystrophies but may manifest later in childhood or adult life (limb-girdle muscular dystrophy (LGMD) 2I, LGMD2K, LGMD2M, LGMD2N, and LGMD2O).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP863668.RAbl6aU_2z_3qLaNtB4mpNiQgfmNndalG45GdTgY0ZEfI130_provenance.
- NP919523.RAcq5spwLfWu-UhuH_WMrGbLwTTY5WBD75FVCzyauLF88130_assertion description "[The secondary ?-dystroglycanopathies usually present in infancy as congenital muscular dystrophies but may manifest later in childhood or adult life (limb-girdle muscular dystrophy (LGMD) 2I, LGMD2K, LGMD2M, LGMD2N, and LGMD2O).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP919523.RAcq5spwLfWu-UhuH_WMrGbLwTTY5WBD75FVCzyauLF88130_provenance.
- NP847973.RAUq-RSagGfCu06_1D5OGROsHmqQ-4oMfVsrWKcc1l9ew130_assertion description "[The secondary ?-dystroglycanopathies usually present in infancy as congenital muscular dystrophies but may manifest later in childhood or adult life (limb-girdle muscular dystrophy (LGMD) 2I, LGMD2K, LGMD2M, LGMD2N, and LGMD2O).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP847973.RAUq-RSagGfCu06_1D5OGROsHmqQ-4oMfVsrWKcc1l9ew130_provenance.
- assertion description "[The secondary ?-dystroglycanopathies usually present in infancy as congenital muscular dystrophies but may manifest later in childhood or adult life (limb-girdle muscular dystrophy (LGMD) 2I, LGMD2K, LGMD2M, LGMD2N, and LGMD2O).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[The secondary ?-dystroglycanopathies usually present in infancy as congenital muscular dystrophies but may manifest later in childhood or adult life (limb-girdle muscular dystrophy (LGMD) 2I, LGMD2K, LGMD2M, LGMD2N, and LGMD2O).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[The secondary ?-dystroglycanopathies usually present in infancy as congenital muscular dystrophies but may manifest later in childhood or adult life (limb-girdle muscular dystrophy (LGMD) 2I, LGMD2K, LGMD2M, LGMD2N, and LGMD2O).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP887423.RAT8dWBnxNvCm-Ic0TfydDwKrt7bLiLBTRMsvvAdUcrnc130_assertion description "[The secondary ?-dystroglycanopathies usually present in infancy as congenital muscular dystrophies but may manifest later in childhood or adult life (limb-girdle muscular dystrophy (LGMD) 2I, LGMD2K, LGMD2M, LGMD2N, and LGMD2O).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP887423.RAT8dWBnxNvCm-Ic0TfydDwKrt7bLiLBTRMsvvAdUcrnc130_provenance.
- NP887425.RATjeGUsgoyVozMyeclhCVACh6NrFdDx34WJvgpDZYEbo130_assertion description "[The secondary ?-dystroglycanopathies usually present in infancy as congenital muscular dystrophies but may manifest later in childhood or adult life (limb-girdle muscular dystrophy (LGMD) 2I, LGMD2K, LGMD2M, LGMD2N, and LGMD2O).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP887425.RATjeGUsgoyVozMyeclhCVACh6NrFdDx34WJvgpDZYEbo130_provenance.
- NP919496.RAosO3HEtgMoKi2woQ9PQ783iYgXn0WTF_qhje7y5r8-k130_assertion description "[The secondary ?-dystroglycanopathies usually present in infancy as congenital muscular dystrophies but may manifest later in childhood or adult life (limb-girdle muscular dystrophy (LGMD) 2I, LGMD2K, LGMD2M, LGMD2N, and LGMD2O).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP919496.RAosO3HEtgMoKi2woQ9PQ783iYgXn0WTF_qhje7y5r8-k130_provenance.
- NP397649.RA8MGmA37M5bPKL1f1Ucbk7wY93ex924fkmzctQlb3Xi8130_assertion description "[The secondary ?-dystroglycanopathies usually present in infancy as congenital muscular dystrophies but may manifest later in childhood or adult life (limb-girdle muscular dystrophy (LGMD) 2I, LGMD2K, LGMD2M, LGMD2N, and LGMD2O).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP397649.RA8MGmA37M5bPKL1f1Ucbk7wY93ex924fkmzctQlb3Xi8130_provenance.
- NP887426.RAKz179u7pG3Sz-0W462-N6azeLcXNPGasDnPB8Lnt8UQ130_assertion description "[The secondary ?-dystroglycanopathies usually present in infancy as congenital muscular dystrophies but may manifest later in childhood or adult life (limb-girdle muscular dystrophy (LGMD) 2I, LGMD2K, LGMD2M, LGMD2N, and LGMD2O).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP887426.RAKz179u7pG3Sz-0W462-N6azeLcXNPGasDnPB8Lnt8UQ130_provenance.
- NP919531.RAyul4rK1k2uOs-U6HdvSpDKfCXZj_0Cpj0ZL2gv98Y0M130_assertion description "[The secondary ?-dystroglycanopathies usually present in infancy as congenital muscular dystrophies but may manifest later in childhood or adult life (limb-girdle muscular dystrophy (LGMD) 2I, LGMD2K, LGMD2M, LGMD2N, and LGMD2O).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP919531.RAyul4rK1k2uOs-U6HdvSpDKfCXZj_0Cpj0ZL2gv98Y0M130_provenance.
- NP887422.RA27F2zEqYRpiABGXlnzkAPmUragdQBPfPuUvOJ2lvc0U130_assertion description "[The secondary ?-dystroglycanopathies usually present in infancy as congenital muscular dystrophies but may manifest later in childhood or adult life (limb-girdle muscular dystrophy (LGMD) 2I, LGMD2K, LGMD2M, LGMD2N, and LGMD2O).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP887422.RA27F2zEqYRpiABGXlnzkAPmUragdQBPfPuUvOJ2lvc0U130_provenance.
- NP887424.RA2A5qY-pbgf7EO-wsSc0vfyo2SuCaDPb6qQJQt1LHHzg130_assertion description "[The secondary ?-dystroglycanopathies usually present in infancy as congenital muscular dystrophies but may manifest later in childhood or adult life (limb-girdle muscular dystrophy (LGMD) 2I, LGMD2K, LGMD2M, LGMD2N, and LGMD2O).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP887424.RA2A5qY-pbgf7EO-wsSc0vfyo2SuCaDPb6qQJQt1LHHzg130_provenance.