High frequency of Q318X mutation in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency in northeast Brazil

Detalhes bibliográficos
Autor(a) principal: Aguiar-Oliveira, Manuel H.
Data de Publicação: 2009
Tipo de documento: Artigo
Idioma: por
Título da fonte: Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Texto Completo: http://www.scielo.br/pdf/abem/v53n1/v53n1a07.pdf
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spelling High frequency of Q318X mutation in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency in northeast BrazilESTEROIDE HIDROXILASE2009info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://www.scielo.br/pdf/abem/v53n1/v53n1a07.pdfhttps:/directbitstream/8da7ef85-4034-4ea0-95f7-129c12da040e/Aguiar-Oliveira, Manuel H.porreponame:Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)instname:Universidade de São Paulo (USP)instacron:USPinfo:eu-repo/semantics/openAccess2024-06-17T15:57:00Z001808032Repositório InstitucionalPUBhttp://www.producao.usp.br/oai/requestopendoar:27212024-06-17T15:57Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual) - Universidade de São Paulo (USP)false
dc.title.none.fl_str_mv High frequency of Q318X mutation in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency in northeast Brazil
title High frequency of Q318X mutation in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency in northeast Brazil
spellingShingle High frequency of Q318X mutation in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency in northeast Brazil
Aguiar-Oliveira, Manuel H.
ESTEROIDE HIDROXILASE
title_short High frequency of Q318X mutation in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency in northeast Brazil
title_full High frequency of Q318X mutation in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency in northeast Brazil
title_fullStr High frequency of Q318X mutation in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency in northeast Brazil
title_full_unstemmed High frequency of Q318X mutation in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency in northeast Brazil
title_sort High frequency of Q318X mutation in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency in northeast Brazil
author Aguiar-Oliveira, Manuel H.
author_facet Aguiar-Oliveira, Manuel H.
author_role author
dc.contributor.author.fl_str_mv Aguiar-Oliveira, Manuel H.
dc.subject.por.fl_str_mv ESTEROIDE HIDROXILASE
topic ESTEROIDE HIDROXILASE
publishDate 2009
dc.date.none.fl_str_mv 2009
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
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dc.identifier.uri.fl_str_mv http://www.scielo.br/pdf/abem/v53n1/v53n1a07.pdf
url http://www.scielo.br/pdf/abem/v53n1/v53n1a07.pdf
dc.language.iso.fl_str_mv por
language por
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