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A Novel Splice-Site Deletion in the POU1F1 Gene Causes Combined Pituitary Hormone Deficiency in Multiple Sudanese Pedigrees.
Hassan, Samar S; Abdullah, Mohamed; Trebusak Podkrajsek, Katarina; Musa, Salwa; Ibrahim, Areej; Babiker, Omer; Kovac, Jernej; Battelino, Tadej; Avbelj Stefanija, Magdalena.
Afiliação
  • Hassan SS; Department of Pediatric Endocrinology and Diabetes, Gaafar Ibn Auf Pediatric Tertiary Hospital, Khartoum 11114, Sudan.
  • Abdullah M; Sudan Childhood Diabetes Center, Khartoum 11111, Sudan.
  • Trebusak Podkrajsek K; Department of Pediatric Endocrinology and Diabetes, Gaafar Ibn Auf Pediatric Tertiary Hospital, Khartoum 11114, Sudan.
  • Musa S; Sudan Childhood Diabetes Center, Khartoum 11111, Sudan.
  • Ibrahim A; Department of Pediatrics, Faculty of Medicine, University of Khartoum, Khartoum 11115, Sudan.
  • Babiker O; Clinical Institute of Special Laboratory Diagnostics, University Children's Hospital, Ljubljana University Medical Centre, 1000 Ljubljana, Slovenia.
  • Kovac J; Faculty of Medicine, University of Ljubljana, 1000 Ljubljana, Slovenia.
  • Battelino T; Department of Pediatric Endocrinology and Diabetes, Gaafar Ibn Auf Pediatric Tertiary Hospital, Khartoum 11114, Sudan.
  • Avbelj Stefanija M; Sudan Childhood Diabetes Center, Khartoum 11111, Sudan.
Genes (Basel) ; 13(4)2022 04 08.
Article em En | MEDLINE | ID: mdl-35456463
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Genes Homeobox / Hipopituitarismo Tipo de estudo: Diagnostic_studies / Etiology_studies / Prognostic_studies Limite: Female / Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Genes Homeobox / Hipopituitarismo Tipo de estudo: Diagnostic_studies / Etiology_studies / Prognostic_studies Limite: Female / Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article