Premium
Congenital myasthenic syndrome type 19 due to a novel mutation in the COL13A1 GENE
Author(s) -
Marquardt Robert J.,
Li Yuebing
Publication year - 2019
Publication title -
muscle and nerve
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.025
H-Index - 145
eISSN - 1097-4598
pISSN - 0148-639X
DOI - 10.1002/mus.26494
Subject(s) - neurology , congenital myasthenic syndrome , medicine , pediatric neurology , clinical neurology , library science , pediatrics , psychology , neuroscience , psychiatry , computer science , receptor , acetylcholine receptor
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom