157th ENMC International Workshop: Patient registries for rare, inherited muscular disorders 25–27 January 2008 Naarden, The Netherlands
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health
Reference32 articles.
1. Current status of gene therapy for muscle diseases;Thirion;Drug News Perspect,2007
2. Human Gene Mutation Database (HGMD): 2003 update;Stenson;Hum Mutat,2003
3. Online Mendelian Inheritance in Man (OMIM), a knowledgebase of human genes and genetic disorders;Hamosh;Nucleic Acids Res,2005
4. DbSNP: the NCBI database of genetic variation;Sherry;Nucleic Acids Res,2001
5. The integrated database for mutations in disease-causing genes: mutation view/KMDB;Ohtsubo;Seikagaku,2003
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