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Digenic DUOX1 and DUOX2 Mutations in Cases With Congenital Hypothyroidism.
Aycan, Zehra; Cangul, Hakan; Muzza, Marina; Bas, Veysel N; Fugazzola, Laura; Chatterjee, V Krishna; Persani, Luca; Schoenmakers, Nadia.
Afiliação
  • Aycan Z; Division of Paediatric Endocrinology, Dr. Sami Ulus Woman Health and Children Research Hospital, 06080 Ankara, Turkey.
  • Cangul H; Department of Medical Genetics, Istanbul Medipol University, International School of Medicine, 34810 Istanbul, Turkey.
  • Muzza M; Endocrine Unit, Fondazione Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Ca' Granda Policlinico, 20122 Milan, Italy.
  • Bas VN; Division of Paediatric Endocrinology, Dr. Sami Ulus Woman Health and Children Research Hospital, 06080 Ankara, Turkey.
  • Fugazzola L; Department of Pathophysiology and Transplantation, University of Milan, 20122 Milan, Italy.
  • Chatterjee VK; Division of Endocrinology and Metabolism, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Istituto Auxologico Italiano, 20149 Milan, Italy.
  • Persani L; University of Cambridge Metabolic Research Laboratories, Wellcome Trust-Medical Research Council Institute of Metabolic Science, Addenbrooke's Hospital, Cambridge CB2 0QQ, United Kingdom.
  • Schoenmakers N; Division of Endocrinology and Metabolism, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Istituto Auxologico Italiano, 20149 Milan, Italy.
J Clin Endocrinol Metab ; 102(9): 3085-3090, 2017 09 01.
Article em En | MEDLINE | ID: mdl-28633507
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: NADPH Oxidases / Predisposição Genética para Doença / Hipotireoidismo Congênito Idioma: En Ano de publicação: 2017 Tipo de documento: Article
Texto completo
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XML
PubMed Links
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: NADPH Oxidases / Predisposição Genética para Doença / Hipotireoidismo Congênito Idioma: En Ano de publicação: 2017 Tipo de documento: Article