Mutations in the gene encoding paired box domain (PAX8) are not a frequent cause of congenital hypothyroidism (CH) in Iranian patients with thyroid dysgenesis;As mutações no gene PAX8 não constituem uma causa frequente de hipotireoidismo congênito em pacientes Iranianos com disgenesia tiroidiana

Arquivos Brasileiros de Endocrinologia e Metabologia

Volumn 54, Issue 6, 2010, Pages 555-559

  Mahjoubi, Frouzandeh ^a   Mohammadi, Mona Malek ^a   Montazeri, Maryam ^a   Aminii, Masoud ^b   Hashemipour, Mahin ^b  

^a NATIONAL INSTITUTE OF GENETIC ENGINEERING AND BIOTECHNOLOGY   (Iran)

^b ISFAHAN UNIVERSITY OF MEDICAL SCIENCES   (Iran)

Author keywords

Congenital hypothyroidism; Gene mutation; PAX8; Thyroid dysgenesis

Indexed keywords

EID: 77957748607     PISSN: 00042730     EISSN: 16779487     Source Type: Journal    
DOI: 10.1590/S0004-27302010000600008     Document Type: Article

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