Identification and mutation analysis of a cochlear-expressed, zinc finger protein gene at the DFNB7/11 and dn hearing-loss loci on human chromosome 9q and mouse chromosome 19.

Scott, D A; Greinwald, J H; Marietta, J R; Drury, S; Swiderski, R E; Viñas, A; DeAngelis, M M; Carmi, R; Ramesh, A; Kraft, M L; Elbedour, K; Skworak, A B; Friedman, R A; Srikumari Srisailapathy, C R; Verhoeven, K; Van Gamp, G; Lovett, M; Deininger, P L; Batzer, M A; Morton, C C; Keats, B J; Smith, R J; Sheffield, V C

Scott, D A; Greinwald, J H; Marietta, J R; Drury, S; Swiderski, R E; Viñas, A; DeAngelis, M M; Carmi, R; Ramesh, A; Kraft, M L; Elbedour, K; Skworak, A B; Friedman, R A; Srikumari Srisailapathy, C R; Verhoeven, K; Van Gamp, G; Lovett, M; Deininger, P L; Batzer, M A; Morton, C C; Keats, B J; Smith, R J; Sheffield, V C.

Affiliation

Scott DA; Department of Pediatrics, University of Iowa Hospitals and Clinics, Iowa City, IA 52242-1078, USA.

Gene ; 215(2): 461-9, 1998 Jul 30.

Article in En | MEDLINE | ID: mdl-9758550

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Collection: 01-internacional Database: MEDLINE Main subject: Chromosomes, Human, Pair 19 / Proteins / Chromosome Mapping / Cochlea / Hearing Loss Type of study: Diagnostic_studies Limits: Animals / Humans Language: En Journal: Gene Year: 1998 Document type: Article Affiliation country: Country of publication:

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