Establishing prevalence in rare neuromuscular diseases A lesson from congenital myopathies

Journal article

Open access

Peer reviewed

Ahmed K. Bamaga and Conrad C. Weihl

Neurology. Genetics, Vol.3(2), pp.e146-e146

01/04/2017

PMID: 28357412

Abstract

Clinical Neurology

Genetics & Heredity

Life Sciences & Biomedicine

Neurosciences & Neurology

Science & Technology

url

https://doi.org/10.1212/NXG.0000000000000146View

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Title: Establishing prevalence in rare neuromuscular diseases A lesson from congenital myopathies
Creators - without role: Ahmed K. Bamaga - Washington University in St. Louis
Conrad C. Weihl - Washington University in St. Louis
Publication Details: Neurology. Genetics, Vol.3(2), pp.e146-e146
Publisher: Lippincott Williams & Wilkins
Number of pages: 2
Grant note: Myositis Association Muscular Dystrophy Association AG031867; AG042095 / Ultragenyx Pharmaceuticals, NIH; United States Department of Health & Human Services; National Institutes of Health (NIH) - USA K02AG042095 / NATIONAL INSTITUTE ON AGING; United States Department of Health & Human Services; National Institutes of Health (NIH) - USA; NIH National Institute on Aging (NIA)
Identifiers: 9935502808331
Academic Unit: King Abdulaziz University
Language: English
Resource Type: Journal article