Genetic basis of congenital hypothyroidism: Abnormalities in the TSHβ gene, the PIT1 gene, and the NIS gene

Clinical Chemistry and Laboratory Medicine

Volumn 36, Issue 8, 1998, Pages 659-662

  Tatsumi, Ke Ita ^a   Miyai, Kiyoshi ^b   Amino, Nobuyuki ^a  

^a OSAKA UNIVERSITY MEDICAL SCHOOL   (Japan)

^b KOSHIEN UNIVERSITY   (Japan)

Author keywords

Hypothyroidism; NIS gene; PIT1 gene; Thyrotropin (TSH); TSH gene

Indexed keywords

DNA BINDING PROTEIN; GROWTH HORMONE; IODIDE; MEMBRANE PROTEIN; PROLACTIN; THYROTROPIN;

CLINICAL ARTICLE; CONFERENCE PAPER; CONGENITAL HYPOTHYROIDISM; CONTROLLED STUDY; GROWTH HORMONE DEFICIENCY; HORMONE DEFICIENCY; HUMAN; HUMAN CELL; MEMBRANE TRANSPORT; MISSENSE MUTATION; PRIORITY JOURNAL; THYROID CELL; THYROID FUNCTION; TRANSACTIVATION;

CARRIER PROTEINS; CONGENITAL HYPOTHYROIDISM; HUMANS; HYPOTHYROIDISM; MEMBRANE PROTEINS; MUTATION; PHOSPHOLIPID TRANSFER PROTEINS; SYMPORTERS; THYROTROPIN;

EID: 0031713949     PISSN: 14346621     EISSN: None     Source Type: Journal    
DOI: 10.1515/CCLM.1998.117     Document Type: Conference Paper

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