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Volumn 215, Issue 2, 1998, Pages 461-469

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

(23)  Scott, D A a   Greinwald Jr , J H a   Marietta, J R a   Drury, S b   Swiderski, R E a   Vinas A b   Deangelis, M M b   Carmi, R c   Ramesh, A d   Kraft, M L a   Elbedour, K c   Skworak, A B e   Friedman, R A f   Srikumari Srisailapathy, C R d   Verhoeven, K g   Van Camp, G g   Lovett, M h   Deininger, P L b   Batzer, M A b   Morton, C C e   more..


Author keywords

Autosomal recessive non syndromic hearing loss; Zinc finger protein

Indexed keywords

COMPLEMENTARY DNA; ZINC FINGER PROTEIN;

EID: 0032581636     PISSN: 03781119     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0378-1119(98)00316-3     Document Type: Article
Times cited : (29)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.