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

We have established strong linkage evidence that supports mapping autosomal-dominant sensory/motor neuropathy with ataxia (SMNA) to chromosome 7q22-q32. SMNA is a rare neurological disorder whose phenotype encompasses both the central and the peripheral nervous system. In order to identify a gene re...

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Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Brkanac, Zoran, Spencer, David, Shendure, Jay, Robertson, Peggy D., Matsushita, Mark, Vu, Tiffany, Bird, Thomas D., Olson, Maynard V., Raskind, Wendy H.
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Elsevier 2009
Gaiak:
Report
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC2680994/
https://ncbi.nlm.nih.gov/pubmed/19409521
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ajhg.2009.04.008
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