Establishing prevalence in rare neuromuscular diseases: A lesson from congenital myopathies

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@article{3203e1092dc244d599e62feec63d6cc9,

title = "Establishing prevalence in rare neuromuscular diseases: A lesson from congenital myopathies",

author = "Bamaga, {Ahmed K.} and Weihl, {Conrad C.}",

year = "2017",

doi = "10.1212/NXG.0000000000000146",

language = "English",

volume = "3",

journal = "Neurology: Genetics",

issn = "2376-7839",

number = "2",

}

TY - JOUR

T1 - Establishing prevalence in rare neuromuscular diseases

T2 - A lesson from congenital myopathies

AU - Bamaga, Ahmed K.

AU - Weihl, Conrad C.

PY - 2017

Y1 - 2017

UR - http://www.scopus.com/inward/record.url?scp=85052668943&partnerID=8YFLogxK

U2 - 10.1212/NXG.0000000000000146

DO - 10.1212/NXG.0000000000000146

M3 - Editorial

C2 - 28357412

AN - SCOPUS:85052668943

SN - 2376-7839

VL - 3

JO - Neurology: Genetics

JF - Neurology: Genetics

IS - 2

M1 - e146

ER -