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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Bibliografiset tiedot
Päätekijät: 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.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Cold Spring Harbor Laboratory Press 1998
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Letters
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC310690/
https://ncbi.nlm.nih.gov/pubmed/9445488
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