Molecular diagnosis of inheritable neuromuscular disorders. Part I: Genetic determinants of inherited disease and their laboratory detection-Reference-Cited by-同舟云学术

Molecular diagnosis of inheritable neuromuscular disorders. Part I: Genetic determinants of inherited disease and their laboratory detection

Published:2005 Issue:4 Volume:31 Page:418-430
ISSN:0148-639X
Container-title:Muscle & Nerve
language:en
Short-container-title:Muscle Nerve

Author:

Greenberg Steven A.,Walsh Ronan J.

Publisher

Wiley

Subject

Physiology (medical),Cellular and Molecular Neuroscience,Neurology (clinical),Physiology

Reference72 articles.

1. Glycyl tRNA Synthetase Mutations in Charcot-Marie-Tooth Disease Type 2D and Distal Spinal Muscular Atrophy Type V

2. The detection of large deletions or duplications in genomic DNA

3. Athena Diagnostics. Policy for billing of commercial insurance. Available at: http://www.athenadiagnostics.com/site/content/resources/billing.asp#Anchor-Commercial-47857.

4. Variability of disease progression in a family with autosomal recessive CMT associated with a S194X and new R310Q mutation in the GDAP1 gene

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