USH1A: chronicle of a slow death - PubMed (original) (raw)
- PMID: 16400615
- PMCID: PMC1380243
- DOI: 10.1086/500275
USH1A: chronicle of a slow death
Sylvie Gerber et al. Am J Hum Genet. 2006 Feb.
No abstract available
References
Web Resources
- GenBank, http://www.ncbi.nlm.nih.gov/GenBank/ (for CCNK [accession numbers AF270825–AF270832], HuEMAP [accession number AJ420603], KNS2 [accession numbers AF267517–AF267531], and myosin VIIA [accession number NM_000260])
- Online Mendelian Inheritance in Man (OMIM), <http:// www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=OMIM/> (for USH1A, USH1B, USH1C, USH1D, USH1E, USH1F, and USH1G)
References
- Cabeza-Arvelaiz Y, Shih LC, Hardman N, Asselbergs F, Bilbe G, Schmitz A, White B, Siciliano MJ, Lachman LB (1993) Cloning and genetic characterization of the human kinesin light-chain (KLC) gene. DNA Cell Biol 12:881–892 - PubMed
- Eudy JD, Ma-Edmonds M, Yao SF, Talmadge CB, Kelley PM, Weston MD, Kimberling WJ, Sumegi J (1997 ) Isolation of a novel human homologue of the gene coding for echinoderm microtubule-associated protein (EMAP) from the Usher syndrome type 1a locus at 14q32. Genomics 43:104–10610.1006/geno.1997.4779 - DOI - PubMed
- Fishman GA, Kumar A, Joseph ME, Torok N, Aderson RJ (1983) Usher’s syndrome: ophthalmic and neuro-otologic findings suggesting genetic heterogeneity. Arch Ophthalmol 101:1367–1374 - PubMed
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