CONGENITAL MYASTHENIC SYNDROMES AND MYASTHENIA: P.70New homozygous mutation in DPAGT1 gene leading to LG-CMS with tubular aggregates.

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Bibliographic Details
Title: CONGENITAL MYASTHENIC SYNDROMES AND MYASTHENIA: P.70New homozygous mutation in DPAGT1 gene leading to LG-CMS with tubular aggregates.
Authors: Gidaro, T.1, Vandenbrande, L.1, Malfatti, E.1, Labasse, C.1, Carlier, P.1, Romero, N.1, Servais, L.1, Böhm, J.2
Source: Neuromuscular Disorders. Oct2018:Supplement 2, Vol. 28, pS51-S51. 1p.
Database: Academic Search Ultimate
Description
ISSN:09608966
DOI:10.1016/j.nmd.2018.06.098