A Positive Modifier of Spinal Muscular Atrophy in the SMN2 Gene-Reference-Cited by-同舟云学术

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A Positive Modifier of Spinal Muscular Atrophy in the SMN2 Gene

Published:2009-09 Issue:3 Volume:85 Page:408-413
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Prior Thomas W.,Krainer Adrian R.,Hua Yimin,Swoboda Kathryn J.,Snyder Pamela C.,Bridgeman Scott J.,Burghes Arthur H.M.,Kissel John T.

Funder

National Institute of Child Health and Human Development

National Center for Research Resources

National Institutes of Health

National Institute of General Medical Sciences

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference29 articles.

1. Incidence, prevalence, and gene frequency studies of chronic childhood spinal muscular atrophy;Pearn;J. Med. Genet.,1978

2. International SMA consortium meeting;Munsat;Neuromuscul. Disord.,1992

3. Natural history in proximal spinal muscular atrophy: clinical analysis of 445 patients and suggestions for a modification of existing classifications;Zerres;Arch. Neurol.,1995

4. Identification and characterization of a spinal muscular atrophy-determining gene;Lefebvre;Cell,1995

5. Genomic variation and gene conversion in spinal muscular atrophy: implications for disease process and clinical phenotype;Campbell;Am. J. Hum. Genet.,1997

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