Matches in Nanopublications for { ?s ?p "[Three genes responsible for hereditary motor and sensory neuropathy type I (HMSNI) or CMT1 have been identified: peripheral myelin protein 22 (PMP22) and myelin protein zero (MPZ) for the autosomal dominant form and connexin 32 (Cx32) for the X-linked dominant variant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP691018.RAAPtRU8-H5h_dPJAnfzRyfx6bk1kEdIGnn3WJB6mjbKM130_assertion description "[Three genes responsible for hereditary motor and sensory neuropathy type I (HMSNI) or CMT1 have been identified: peripheral myelin protein 22 (PMP22) and myelin protein zero (MPZ) for the autosomal dominant form and connexin 32 (Cx32) for the X-linked dominant variant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP691018.RAAPtRU8-H5h_dPJAnfzRyfx6bk1kEdIGnn3WJB6mjbKM130_provenance.
- NP806841.RADX462guOji1aOceNmVFJqR1owWJelMwLTK5Wr1KtYug130_assertion description "[Three genes responsible for hereditary motor and sensory neuropathy type I (HMSNI) or CMT1 have been identified: peripheral myelin protein 22 (PMP22) and myelin protein zero (MPZ) for the autosomal dominant form and connexin 32 (Cx32) for the X-linked dominant variant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP806841.RADX462guOji1aOceNmVFJqR1owWJelMwLTK5Wr1KtYug130_provenance.
- NP352279.RAdwOEEYBHlkVmw4jJ-0NRdvwfQjx0PPyds-YmRiRhm_U130_assertion description "[Three genes responsible for hereditary motor and sensory neuropathy type I (HMSNI) or CMT1 have been identified: peripheral myelin protein 22 (PMP22) and myelin protein zero (MPZ) for the autosomal dominant form and connexin 32 (Cx32) for the X-linked dominant variant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP352279.RAdwOEEYBHlkVmw4jJ-0NRdvwfQjx0PPyds-YmRiRhm_U130_provenance.
- NP426192.RAnpNhWAn-Ot4ZoW7ZN4ohZhrzxm_wIGeqE1WZLcRFe9w130_assertion description "[Three genes responsible for hereditary motor and sensory neuropathy type I (HMSNI) or CMT1 have been identified: peripheral myelin protein 22 (PMP22) and myelin protein zero (MPZ) for the autosomal dominant form and connexin 32 (Cx32) for the X-linked dominant variant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP426192.RAnpNhWAn-Ot4ZoW7ZN4ohZhrzxm_wIGeqE1WZLcRFe9w130_provenance.
- NP294326.RAjzMnvqnFCBDjyZMy-3mbGGWJw40NcbDU19QcaZUHMUQ130_assertion description "[Three genes responsible for hereditary motor and sensory neuropathy type I (HMSNI) or CMT1 have been identified: peripheral myelin protein 22 (PMP22) and myelin protein zero (MPZ) for the autosomal dominant form and connexin 32 (Cx32) for the X-linked dominant variant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP294326.RAjzMnvqnFCBDjyZMy-3mbGGWJw40NcbDU19QcaZUHMUQ130_provenance.
- NP294327.RAvIjsE8OdSvlP6F3uCw1XgVQnJhxBpQVfnYeOIn_3yIM130_assertion description "[Three genes responsible for hereditary motor and sensory neuropathy type I (HMSNI) or CMT1 have been identified: peripheral myelin protein 22 (PMP22) and myelin protein zero (MPZ) for the autosomal dominant form and connexin 32 (Cx32) for the X-linked dominant variant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP294327.RAvIjsE8OdSvlP6F3uCw1XgVQnJhxBpQVfnYeOIn_3yIM130_provenance.
- NP568356.RAEr4OBhs6NiWQCZ0fFiEyETGaEFKGFALoobJO1JK7KBk130_assertion description "[Three genes responsible for hereditary motor and sensory neuropathy type I (HMSNI) or CMT1 have been identified: peripheral myelin protein 22 (PMP22) and myelin protein zero (MPZ) for the autosomal dominant form and connexin 32 (Cx32) for the X-linked dominant variant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP568356.RAEr4OBhs6NiWQCZ0fFiEyETGaEFKGFALoobJO1JK7KBk130_provenance.
- NP294325.RAy3WSJzZS-QlpJ_dMMFb4eTVHmmkc2fYZ8hriBztcHv0130_assertion description "[Three genes responsible for hereditary motor and sensory neuropathy type I (HMSNI) or CMT1 have been identified: peripheral myelin protein 22 (PMP22) and myelin protein zero (MPZ) for the autosomal dominant form and connexin 32 (Cx32) for the X-linked dominant variant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP294325.RAy3WSJzZS-QlpJ_dMMFb4eTVHmmkc2fYZ8hriBztcHv0130_provenance.