Caracterização molecular do gene TPO em crianças Portuguesas com hipotiroidismo congénito causado por disormonogénese

Congenital hypothyroidism (CH) affects about 1:4000 infants and is considered one of the main causes of preventable mental retardation in children. Universal screening of CH performed through the Portuguese National Neonatal Screening Programme, implemented in Portugal in 1985, has resulted in norma...

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Bibliographic Details
Main Author: Nogueira, Célia (author)
Other Authors: Vaz Osório, Rui (author), Santos, Rosário (author), Jorge, Paula (author)
Format: article
Language:por
Published: 2012
Subjects:
Hipotiroidismo Congénito
Disormonogénese
Gene TPO
Espectro Mutacional
Peroxidase da Tiroide
Doenças Genéticas
Online Access:http://hdl.handle.net/10400.18/606
Country:Portugal
Oai:oai:repositorio.insa.pt:10400.18/606

Internet

http://hdl.handle.net/10400.18/606

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