Spectrum of human Foxe1/TTF-2 mutations

Hormone Research in Paediatrics

Volumn 73, Issue 6, 2010, Pages 423-429

  Castanet, Mireille ^a   Polak, Michel ^a  

^a INSERM   (France)

Author keywords

Bamforth syndrome; Congenital hypothyroidism; Thyroid dysgenesis

Indexed keywords

ARGININE; ASPARAGINE; CYSTEINE; POLYALANINE; POLYAMINOACID; SERINE; THYROGLOBULIN; THYROID TRANSCRIPTION FACTOR 2; TRANSCRIPTION FACTOR FORKHEAD BOX E1; TRANSCRIPTION FACTOR FOXE1; UNCLASSIFIED DRUG;

AMINO ACID SUBSTITUTION; BAMFORTH SYNDROME; CELL MIGRATION; CHOANA ATRESIA; CLEFT PALATE; CONGENITAL HYPOTHYROIDISM; CONSANGUINITY; ECHOGRAPHY; EPIGLOTTIS; GENE EXPRESSION; GENE MUTATION; GENETIC DISORDER; HETEROZYGOTE; HOMOZYGOSITY; HUMAN; INHERITANCE; LOSS OF FUNCTION MUTATION; MISSENSE MUTATION; ORGANOGENESIS; PARENT; PRIORITY JOURNAL; SHORT SURVEY; THYROID DEVELOPMENT; THYROID DYSGENESIS; THYROID FOLLICLE CELL; THYROID FUNCTION; UNIPARENTAL DISOMY;

CLEFT PALATE; FORKHEAD TRANSCRIPTION FACTORS; GENETIC PREDISPOSITION TO DISEASE; HUMANS; MUTATION; THYROID DYSGENESIS;

EID: 77952304081     PISSN: 16632818     EISSN: 16632826     Source Type: Journal    
DOI: 10.1159/000281438     Document Type: Short Survey

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