High frequency of the deafness-associated 167delT mutation in the connexin 26 (GJB2) gene in Israeli Ashkenazim [2]

American Journal of Medical Genetics

Volumn 86, Issue 5, 1999, Pages 499-500

  Sobe, T ^a   Erlich, P ^a   Berry, A ^a   Korostichevsky, M ^a   Vreugde, S ^a   Avraham, K B ^a   Bonne Tamir, B ^a   Shohat, M ^a  

^a TEL AVIV UNIVERSITY   (Israel)

Author keywords

[No Author keywords available]

Indexed keywords

GAP JUNCTION PROTEIN;

GENE MUTATION; GENETIC LINKAGE; GENETIC SUSCEPTIBILITY; HEARING IMPAIRMENT; HUMAN; JEW; LETTER; PRIORITY JOURNAL;

CHROMOSOME MAPPING; CONNEXINS; DEAFNESS; EUROPE; GENETIC MARKERS; HETEROZYGOTE DETECTION; HUMANS; ISRAEL; JEWS; SEQUENCE DELETION; THYMINE;

EID: 0033615567     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19991029)86:5<499::AID-AJMG19>3.0.CO;2-O     Document Type: Letter

References (11)