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Clinical and molecular characteristics of congenital hypothyroidism with DUOX2 mutations

Detalles Bibliográficos
Autores principales:	Kim, Yoo-Mi, Jin, Hye Young, Lee, Beom Hee, Heo, Sun-Hee, Kim, Gu-Hwan, Yoo, Han-Wook
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2013
Materias:	Oral Presentation
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3849924/ http://dx.doi.org/10.1186/1687-9856-2013-S1-O54

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