IFRD1 Is a Candidate Gene for SMNA on Chromosome 7q22-q23-Reference-Cited by-同舟云学术

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IFRD1 Is a Candidate Gene for SMNA on Chromosome 7q22-q23

Published:2009-05 Issue:5 Volume:84 Page:692-697
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Brkanac Zoran,Spencer David,Shendure Jay,Robertson Peggy D.,Matsushita Mark,Vu Tiffany,Bird Thomas D.,Olson Maynard V.,Raskind Wendy H.

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference28 articles.

1. Autosomal dominant sensory/motor neuropathy with Ataxia (SMNA): Linkage to chromosome 7q22-q32;Brkanac;Am. J. Med. Genet.,2002

2. Bird TD Hereditary Ataxia Overview.

3. Missense mutations in the regulatory domain of PKC gamma: A new mechanism for dominant nonepisodic cerebellar ataxia;Chen;Am. J. Hum. Genet.,2003

4. Direct selection of human genomic loci by microarray hybridization;Albert;Nat. Methods,2007

5. Mapping short DNA sequencing reads and calling variants using mapping quality scores;Li;Genome Res.,2008

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