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MPZL2 is a novel gene associated with autosomal recessive nonsyndromic moderate hearing loss.
Bademci, Guney; Abad, Clemer; Incesulu, Armagan; Rad, Abolfazl; Alper, Ozgul; Kolb, Susanne M; Cengiz, Filiz B; Diaz-Horta, Oscar; Silan, Fatma; Mihci, Ercan; Ocak, Emre; Najafi, Maryam; Maroofian, Reza; Yilmaz, Elanur; Nur, Banu G; Duman, Duygu; Guo, Shengru; Sant, David W; Wang, Gaofeng; Monje, Paula V; Haaf, Thomas; Blanton, Susan H; Vona, Barbara; Walz, Katherina; Tekin, Mustafa.
Afiliación
  • Bademci G; John P. Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, 1501 NW 10th Avenue, BRB-610 (M-860), Miami, FL, 33136, USA.
  • Abad C; John P. Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, 1501 NW 10th Avenue, BRB-610 (M-860), Miami, FL, 33136, USA.
  • Incesulu A; Department of Otorhinolaryngology, Faculty of Medicine, Eskisehir Osmangazi University, 26040, Eskisehir, Turkey.
  • Rad A; Cellular and Molecular Research Center, Sabzevar University of Medical Sciences, Sabzevar, 009851, Iran.
  • Alper O; Department of Medical Biology and Genetics, Faculty of Medicine, Akdeniz University, 07070, Antalya, Turkey.
  • Kolb SM; Institute of Human Genetics, Julius Maximilians University Würzburg, 97074, Würzburg, Germany.
  • Cengiz FB; John P. Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, 1501 NW 10th Avenue, BRB-610 (M-860), Miami, FL, 33136, USA.
  • Diaz-Horta O; John P. Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, 1501 NW 10th Avenue, BRB-610 (M-860), Miami, FL, 33136, USA.
  • Silan F; Department of Medical Genetics, Canakkale Onsekiz Mart University School of Medicine, 17100, Canakkale, Turkey.
  • Mihci E; Department of Pediatric Genetics, Akdeniz University School of Medicine, 07070, Antalya, Turkey.
  • Ocak E; Department of Otolaryngology, Ankara University School of Medicine, 06260, Ankara, Turkey.
  • Najafi M; Genome Research Division, Human Genetics Department, Radboud University Medical Center, Geert Grooteplein Zuid 10, 6525 KL, Nijmegen, The Netherlands.
  • Maroofian R; Genetics and Molecular Cell Sciences Research Centre, St George's, University of London, Cranmer Terrace, London, SW17 0RE, UK.
  • Yilmaz E; Department of Medical Biology and Genetics, Faculty of Medicine, Akdeniz University, 07070, Antalya, Turkey.
  • Nur BG; Department of Pediatric Genetics, Akdeniz University School of Medicine, 07070, Antalya, Turkey.
  • Duman D; Division of Genetics, Department of Pediatrics, Ankara University School of Medicine, 06260, Ankara, Turkey.
  • Guo S; John P. Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, 1501 NW 10th Avenue, BRB-610 (M-860), Miami, FL, 33136, USA.
  • Sant DW; John P. Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, 1501 NW 10th Avenue, BRB-610 (M-860), Miami, FL, 33136, USA.
  • Wang G; John P. Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, 1501 NW 10th Avenue, BRB-610 (M-860), Miami, FL, 33136, USA.
  • Monje PV; Sylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, Miami, FL, 33136, USA.
  • Haaf T; The Miami Project to Cure Paralysis and the Department of Neurological Surgery, University of Miami Miller School of Medicine, Miami, FL, 33136, USA.
  • Blanton SH; Institute of Human Genetics, Julius Maximilians University Würzburg, 97074, Würzburg, Germany.
  • Vona B; John P. Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, 1501 NW 10th Avenue, BRB-610 (M-860), Miami, FL, 33136, USA.
  • Walz K; Department of Otolaryngology, University of Miami Miller School of Medicine, Miami, FL, 33136, USA.
  • Tekin M; Dr. John T. Macdonald Department of Human Genetics, University of Miami Miller School of Medicine, Miami, FL, 33136, USA.
Hum Genet ; 137(6-7): 479-486, 2018 Jul.
Article en En | MEDLINE | ID: mdl-29982980
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Moléculas de Adhesión Celular / Sordera / Células Ciliadas Auditivas Internas / Pérdida Auditiva Sensorineural Tipo de estudio: Risk_factors_studies Límite: Animals / Female / Humans / Male País/Región como asunto: Asia Idioma: En Revista: Hum Genet Año: 2018 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Alemania
Texto completo
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XML
PubMed Links
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Moléculas de Adhesión Celular / Sordera / Células Ciliadas Auditivas Internas / Pérdida Auditiva Sensorineural Tipo de estudio: Risk_factors_studies Límite: Animals / Female / Humans / Male País/Región como asunto: Asia Idioma: En Revista: Hum Genet Año: 2018 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Alemania