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Ehlers-Danlos Syndrome Caused by Biallelic TNXB Variants in Patients with Congenital Adrenal Hyperplasia.
Chen, Wuyan; Perritt, Ashley F; Morissette, Rachel; Dreiling, Jennifer L; Bohn, Markus-Frederik; Mallappa, Ashwini; Xu, Zhi; Quezado, Martha; Merke, Deborah P.
Afiliação
  • Chen W; PreventionGenetics, Marshfield, Wisconsin.
  • Perritt AF; National Institutes of Health Clinical Center, Bethesda, Maryland.
  • Morissette R; National Institutes of Health Clinical Center, Bethesda, Maryland.
  • Dreiling JL; Laboratory of Pathology, National Cancer Institute, Bethesda, Maryland.
  • Bohn MF; Department of Pharmaceutical Chemistry, University of California San Francisco, San Francisco, California.
  • Mallappa A; National Institutes of Health Clinical Center, Bethesda, Maryland.
  • Xu Z; National Institutes of Health, , National Institute on Aging, Baltimore, Maryland.
  • Quezado M; Laboratory of Pathology, National Cancer Institute, Bethesda, Maryland.
  • Merke DP; National Institutes of Health Clinical Center, Bethesda, Maryland.
Hum Mutat ; 37(9): 893-7, 2016 09.
Article em En | MEDLINE | ID: mdl-27297501
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Esteroide 21-Hidroxilase / Deleção de Genes / Hiperplasia Suprarrenal Congênita / Tenascina / Síndrome de Ehlers-Danlos Tipo de estudo: Prognostic_studies Limite: Adolescent / Adult / Female / Humans / Male Idioma: En Ano de publicação: 2016 Tipo de documento: Article
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Esteroide 21-Hidroxilase / Deleção de Genes / Hiperplasia Suprarrenal Congênita / Tenascina / Síndrome de Ehlers-Danlos Tipo de estudo: Prognostic_studies Limite: Adolescent / Adult / Female / Humans / Male Idioma: En Ano de publicação: 2016 Tipo de documento: Article