Autosomal dominant Emery-Dreifuss muscular dystrophy caused by a mutation in the lamin A/C gene identified by exome sequencing: a case report

Autosomal dominant Emery-Dreifuss muscular dystrophy caused by a mutation in the lamin A/C gene identified by exome sequencing: a case report

10.1186/s12887-022-03662-y

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Bibliographic Details
Main Authors:	Iskandar, K, Sunartini, Astari, FN, Gumilang, RA, Ilma, N, Shartyanie, NP, Adistyawan, G, Tan, G, Gunadi, Lai, PS
Other Authors:	PAEDIATRICS
Format:	Article
Published:	Springer Science and Business Media LLC 2022
Subjects:	Case report Emery-Dreifuss muscular dystrophy Exome sequencing LMNA Laminopathies Autosomal Emery-Dreifuss Muscular Dystrophy Exome Humans Infant Lamin Type A Male Muscle, Skeletal Muscular Dystrophies Muscular Dystrophy, Emery-Dreifuss Mutation
Online Access:	https://scholarbank.nus.edu.sg/handle/10635/234746
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Institution:	National University of Singapore

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