Novel deletion alleles carrying <it>CYP21A1P</it>/<it>A2 </it>chimeric genes in Brazilian patients with 21-hydroxylase deficiency

Novel deletion alleles carrying <it>CYP21A1P</it>/<it>A2 </it>chimeric genes in Brazilian patients with 21-hydroxylase deficiency

<p>Abstract</p> <p>Background</p> <p>Congenital adrenal hyperplasia due to 21-hydroxylase deficiency is caused by deletions, large gene conversions or mutations in <it>CYP21A2 </it>gene. The human gene is located at 6p21.3 within a <it>locus </it>...

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Main Authors: Guerra-Júnior Gil, Baptista Maria TM, de Lemos-Marini Sofia HV, Petroli Reginaldo J, Lau Ivy F, Paulino Luciana C, de Araújo Marcela, Bernardi Renan D, Soardi Fernanda C, Coeli Fernanda B, de-Mello Maricilda P
Format: Article
Language:English
Published: BMC 2010-06-01
Series:BMC Medical Genetics
Online Access:http://www.biomedcentral.com/1471-2350/11/104

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http://www.biomedcentral.com/1471-2350/11/104

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