High frequency of D727E polymorphisms in exon 10 of the TSHR Gene in Brazilian patients with congenital hypothyroidism

Journal of Pediatric Endocrinology and Metabolism

Volumn 23, Issue 12, 2010, Pages 1321-1328

  Alves, Erik A C ^a   Cruz, Cleber M ^a   Pimentel, Clebson P ^a   Ribeiro, Rita C M ^a   Santos, Andrea K C R ^a   Caldato, Milena C F ^b   Santana Da Silva, Luiz C ^a  

^a FEDERAL UNIVERSITY OF PARÁ   (Brazil)

^b Departamento de Patologia   (Brazil)

Author keywords

Congenital hypothyroidism; D727E; Plymorphism; Receptor thyrotropin; Thyroid

Indexed keywords

ALANINE; ASPARTIC ACID; GENOMIC DNA; GLUTAMIC ACID; LEUCINE; THYROTROPIN RECEPTOR;

ALLELE; AMINO ACID SEQUENCE; AMPLICON; ARTICLE; BRAZIL; CHILD; CONGENITAL HYPOTHYROIDISM; CONTROLLED STUDY; DNA ISOLATION; DNA POLYMORPHISM; EXON; FEMALE; GENE AMPLIFICATION; GENE FREQUENCY; GENE MUTATION; HUMAN; MAJOR CLINICAL STUDY; MALE; POLYMERASE CHAIN REACTION; PRESCHOOL CHILD; SCHOOL CHILD;

BRAZIL; CHILD; CHILD, PRESCHOOL; CONGENITAL HYPOTHYROIDISM; EXONS; FEMALE; HUMANS; INFANT; MALE; POLYMORPHISM, GENETIC; RECEPTORS, THYROTROPIN;

EID: 79955509430     PISSN: 0334018X     EISSN: None     Source Type: Journal    
DOI: 10.1515/jpem.2010.206     Document Type: Article

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