Thyroid peroxidase gene mutations causing congenital hypothyroidism in three Turkish families

Journal of Pediatric Endocrinology and Metabolism

Volumn 22, Issue 11, 2009, Pages 1033-1039

  Ozbek, Mehmet Nuri ^a   Uslu, Abdi Burak ^a   Onenli Mungan, Neslihan ^a   Yuksel, Bilgin ^a   Pohlenz, Joachim ^b   Topaloglu, Ali Kemal ^a  

^a CUKUROVA UNIVERSITY   (Turkey)

^b JOHANNES GUTENBERG UNIVERSITY   (Germany)

Author keywords

Congenital hypothyroidism; Dyshormonogenesis; Mutation; Thyroid peroxidase gene

Indexed keywords

LEVOTHYROXINE; THYROGLOBULIN; THYROID PEROXIDASE; THYROTROPIN; THYROXINE;

ARTICLE; CHILD; CLINICAL ARTICLE; CLINICAL FEATURE; CONGENITAL HYPOTHYROIDISM; CONSANGUINITY; EXON; FEMALE; GENE IDENTIFICATION; GENE MUTATION; GENOTYPE; GOITER; HAPLOTYPE; HUMAN; INFANT; MACROGLOSSIA; MALE; MUTATIONAL ANALYSIS; NEWBORN JAUNDICE; NONSENSE MUTATION; PATIENT COMPLIANCE; PRESCHOOL CHILD; SCHOOL CHILD; THYROGLOBULIN BLOOD LEVEL; THYROTROPIN BLOOD LEVEL; THYROXINE BLOOD LEVEL; TURKEY (REPUBLIC);

EID: 75749126574     PISSN: 0334018X     EISSN: None     Source Type: Journal    
DOI: 10.1515/JPEM.2009.22.11.1033     Document Type: Article

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