Congenital hypothyroidism caused by mutations in the thyrotropin- receptor gene [5]

New England Journal of Medicine

Volumn 336, Issue 19, 1997, Pages 1390-1391

  Biebermann, H ^a   Gruters, A ^a   Schoneberg, T ^a   Gudermann, T ^a  

^a HUMBOLDT UNIVERSITY   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

THYROTROPIN RECEPTOR; THYROXINE;

CASE REPORT; CONGENITAL HYPOTHYROIDISM; CONTROLLED STUDY; ELECTROPHORETIC MOBILITY; FREE THYROXINE INDEX; GENE MUTATION; HUMAN; HUMAN CELL; HYPOPLASIA; LETTER; POLYMERASE CHAIN REACTION; PRESCHOOL CHILD; PRIORITY JOURNAL; SINGLE STRAND CONFORMATION POLYMORPHISM; THYROTROPIN BLOOD LEVEL;

CONGENITAL HYPOTHYROIDISM; GERM-LINE MUTATION; HUMANS; HYPOTHYROIDISM; INFANT, NEWBORN; RECEPTORS, THYROTROPIN; THYROID GLAND;

EID: 0030901754     PISSN: 00284793     EISSN: None     Source Type: Journal    
DOI: 10.1056/NEJM199705083361914     Document Type: Letter

References (1)