Matches in Nanopublications for { ?s ?p "[Identification of DPAGT1, ALG14 and ALG2 mutations as a cause of congenital myasthenic syndrome underscores the importance of asparagine-linked protein glycosylation for proper functioning of the neuromuscular junction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP222772.RACj9yxd_aIbHAhB3K364OskETJkcvLJ_6s4SeTOhhaL0130_assertion description "[Identification of DPAGT1, ALG14 and ALG2 mutations as a cause of congenital myasthenic syndrome underscores the importance of asparagine-linked protein glycosylation for proper functioning of the neuromuscular junction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP222772.RACj9yxd_aIbHAhB3K364OskETJkcvLJ_6s4SeTOhhaL0130_provenance.
- NP396581.RAQLMFEeIcwxluv0UVcfuxQ9X4g6gqOIZxUPyslCHdaF4130_assertion description "[Identification of DPAGT1, ALG14 and ALG2 mutations as a cause of congenital myasthenic syndrome underscores the importance of asparagine-linked protein glycosylation for proper functioning of the neuromuscular junction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP396581.RAQLMFEeIcwxluv0UVcfuxQ9X4g6gqOIZxUPyslCHdaF4130_provenance.
- NP537184.RAtG4nebKEKD9zn46NBGxg9KPFG-8R-Xn_lRh2ibGRt44130_assertion description "[Identification of DPAGT1, ALG14 and ALG2 mutations as a cause of congenital myasthenic syndrome underscores the importance of asparagine-linked protein glycosylation for proper functioning of the neuromuscular junction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP537184.RAtG4nebKEKD9zn46NBGxg9KPFG-8R-Xn_lRh2ibGRt44130_provenance.
- NP682830.RAF_55y6ArOZtkpL-Zqg03K8RWuOmJybqo-QHvGixSPUA130_assertion description "[Identification of DPAGT1, ALG14 and ALG2 mutations as a cause of congenital myasthenic syndrome underscores the importance of asparagine-linked protein glycosylation for proper functioning of the neuromuscular junction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP682830.RAF_55y6ArOZtkpL-Zqg03K8RWuOmJybqo-QHvGixSPUA130_provenance.
- NP358368.RAIAcjy9srTH78cO6V6LWKe8xoRzFlNahQhTVwFbXEyDU130_assertion description "[Identification of DPAGT1, ALG14 and ALG2 mutations as a cause of congenital myasthenic syndrome underscores the importance of asparagine-linked protein glycosylation for proper functioning of the neuromuscular junction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP358368.RAIAcjy9srTH78cO6V6LWKe8xoRzFlNahQhTVwFbXEyDU130_provenance.
- NP1052512.RA8u-BR5ZeTSSCRlfiPRHW1HpjoDcUEFRme-FV88-DbVY130_assertion description "[Identification of DPAGT1, ALG14 and ALG2 mutations as a cause of congenital myasthenic syndrome underscores the importance of asparagine-linked protein glycosylation for proper functioning of the neuromuscular junction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1052512.RA8u-BR5ZeTSSCRlfiPRHW1HpjoDcUEFRme-FV88-DbVY130_provenance.