Congenital hypothyroidism caused by a mutation in the Na+/l - symporter

Nature Genetics

Volumn 16, Issue 2, 1997, Pages 124-125

  Fujiwara, Hirokazu ^a   Tatsumi, Ke Ita ^a   Miki, Kazunori ^a   Harada, Tokuzo ^a   Miyai, Kiyoshi ^a   Takai, Shin Ichiro ^b   Amino, Nobuyuki ^a  

^a KOSHIEN UNIVERSITY   (Japan)

^b OSAKA UNIVERSITY MEDICAL SCHOOL   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

CARRIER PROTEIN; COTRANSPORTER; MEMBRANE PROTEIN; SODIUM IODIDE SYMPORTER;

AMINO ACID SEQUENCE; ANIMAL; CASE REPORT; CELL LINE; CONGENITAL HYPOTHYROIDISM; FEMALE; GENETICS; HOMOZYGOTE; HUMAN; HYPOTHYROIDISM; LETTER; MOLECULAR GENETICS; MUTATION; PEDIGREE; SEQUENCE HOMOLOGY;

AMINO ACID SEQUENCE; ANIMALS; CARRIER PROTEINS; CELL LINE; CONGENITAL HYPOTHYROIDISM; FEMALE; HOMOZYGOTE; HUMANS; HYPOTHYROIDISM; MEMBRANE PROTEINS; MOLECULAR SEQUENCE DATA; MUTATION; PEDIGREE; SEQUENCE HOMOLOGY, AMINO ACID; SYMPORTERS;

EID: 0031156646     PISSN: 10614036     EISSN: None     Source Type: Journal    
DOI: 10.1038/ng0697-124     Document Type: Conference Paper

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