Pendred syndrome maps to chromosome 7q21-34 and is caused by an intrinsic defect in thyroid iodine organification

Nature Genetics

Volumn 12, Issue 4, 1996, Pages 424-426

  Sheffield, Val C ^a   Kraiem, Zaki ^c,d   Beck, John C ^a   Nishimura, Darryl ^a   Stone, Edwin M ^b   Salameh, Muhamad ^e   Sadeh, Orit ^c   Glaser, Benjamin ^e  

^a UNIVERSITY OF IOWA   (United States)

^b UNIVERSITY OF IOWA   (United States)

^c CARMEL MEDICAL CENTER   (Israel)

^d TECHNION ISRAEL INSTITUTE OF TECHNOLOGY   (Israel)

^e HADASSAH HEBREW UNIVERSITY MEDICAL CENTER   (Israel)

Author keywords

[No Author keywords available]

Indexed keywords

IODINE;

ARTICLE; CHROMOSOME 7Q; CHROMOSOME MAP; CONGENITAL DEAFNESS; DNA FLANKING REGION; GENETIC LINKAGE; GENETIC ORGANIZATION; HUMAN; PENDRED SYNDROME; PRIORITY JOURNAL; TANDEM REPEAT; THYROID DISEASE;

CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 7; DEAFNESS; FEMALE; GENETIC MARKERS; GOITER; HUMANS; IODIDE PEROXIDASE; IODINE; LINKAGE (GENETICS); MALE; PEDIGREE; SYNDROME; THYROGLOBULIN; THYROID GLAND;

EID: 0029963073     PISSN: 10614036     EISSN: None     Source Type: Journal    
DOI: 10.1038/ng0496-424     Document Type: Article

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