Contig Maps and Genomic Sequencing Identify Candidate Genes in the Usher 1C Locus

Usher syndrome 1C (USH1C) is a congenital condition manifesting profound hearing loss, the absence of vestibular function, and eventual retinal degeneration. The USH1C locus has been mapped genetically to a 2- to 3-cM interval in 11p14–15.1 between D11S899 and D11S861. In an effort to identify the U...

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Detaylı Bibliyografya
Asıl Yazarlar: Higgins, Michael J., Day, Colleen D., Smilinich, Nancy J., Ni, L., Cooper, Paul R., Nowak, Norma J., Davies, Chris, de Jong, Pieter J., Hejtmancik, Fielding, Evans, Glen A., Smith, Richard J.H., Shows, Thomas B.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Cold Spring Harbor Laboratory Press 1998
Konular:
Letters
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC310690/
https://ncbi.nlm.nih.gov/pubmed/9445488
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