Characterization of mutations in the FOXE1 gene in a cohort of unrelated malaysian patients with congenital hypothyroidism and thyroid dysgenesis

Biochemical Genetics

Volumn 48, Issue 1-2, 2010, Pages 141-151

  Kang, In Nee ^a   Musa, Maslinda ^a   Harun, Fatimah ^a   Junit, Sarni Mat ^a  

^a UNIVERSITY OF MALAYA   (Malaysia)

Author keywords

Congenital hypothyroidism; FOXE1 gene; N132D mutation

Indexed keywords

FORKHEAD BOX PROTEIN E1; FORKHEAD TRANSCRIPTION FACTOR; UNCLASSIFIED DRUG;

ARTICLE; CASE REPORT; COHORT ANALYSIS; CONGENITAL HYPOTHYROIDISM; CONTROLLED STUDY; GENE MUTATION; HUMAN; HUMAN CELL; MALAYSIA; MUTANT; NUCLEOTIDE SEQUENCE; PROMOTER REGION; THYROID DYSGENESIS; WILD TYPE;

ADENINE; AMINO ACID SEQUENCE; ANIMALS; COHORT STUDIES; CONGENITAL ABNORMALITIES; DNA PRIMERS; FORKHEAD TRANSCRIPTION FACTORS; GENE AMPLIFICATION; GENES, REPORTER; GUANINE; HEP G2 CELLS; HUMANS; HYPOTHYROIDISM; MALAYSIA; MOLECULAR SEQUENCE DATA; MUTATION; POLYMERASE CHAIN REACTION; POLYMORPHISM, SINGLE NUCLEOTIDE; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; PROMOTER REGIONS, GENETIC; REFERENCE VALUES; SEQUENCE ALIGNMENT; SEQUENCE HOMOLOGY, AMINO ACID; THYROID DYSGENESIS; TRANSFECTION;

EID: 75949115911     PISSN: 00062928     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10528-009-9306-7     Document Type: Article

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