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Loss-of-Function Mutations in the WNT Co-receptor LRP6 Cause Autosomal-Dominant Oligodontia.
Massink, Maarten P G; Créton, Marijn A; Spanevello, Francesca; Fennis, Willem M M; Cune, Marco S; Savelberg, Sanne M C; Nijman, Isaäc J; Maurice, Madelon M; van den Boogaard, Marie-José H; van Haaften, Gijs.
Afiliación
  • Massink MP; Department of Medical Genetics, Centre for Molecular Medicine, University Medical Centre Utrecht, 3508 AB Utrecht, the Netherlands.
  • Créton MA; Department of Oral and Maxillofacial Surgery, Prosthodontics and Special Dental Care, University Medical Centre Utrecht, 3508 AB Utrecht, the Netherlands.
  • Spanevello F; Department of Cell Biology, Centre for Molecular Medicine, University Medical Centre Utrecht, 3584 CX Utrecht, the Netherlands.
  • Fennis WM; Department of Oral and Maxillofacial Surgery, Prosthodontics and Special Dental Care, University Medical Centre Utrecht, 3508 AB Utrecht, the Netherlands.
  • Cune MS; Department of Fixed and Removable Prosthodontics, Centre for Dentistry and Oral Hygiene, University Medical Centre Groningen, 9700 RB Groningen, the Netherlands; Antonius Hospital, 3435 CM Nieuwegein, the Netherlands.
  • Savelberg SM; Department of Medical Genetics, Centre for Molecular Medicine, University Medical Centre Utrecht, 3508 AB Utrecht, the Netherlands.
  • Nijman IJ; Department of Medical Genetics, Centre for Molecular Medicine, University Medical Centre Utrecht, 3508 AB Utrecht, the Netherlands.
  • Maurice MM; Department of Cell Biology, Centre for Molecular Medicine, University Medical Centre Utrecht, 3584 CX Utrecht, the Netherlands.
  • van den Boogaard MJ; Department of Medical Genetics, Centre for Molecular Medicine, University Medical Centre Utrecht, 3508 AB Utrecht, the Netherlands.
  • van Haaften G; Department of Medical Genetics, Centre for Molecular Medicine, University Medical Centre Utrecht, 3508 AB Utrecht, the Netherlands. Electronic address: g.vanhaaften@umcutrecht.nl.
Am J Hum Genet ; 97(4): 621-6, 2015 Oct 01.
Article en En | MEDLINE | ID: mdl-26387593
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Proteínas Wnt / Proteína-6 Relacionada a Receptor de Lipoproteína de Baja Densidad / Exoma / Genes Dominantes / Anodoncia / Mutación Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Male Idioma: En Revista: Am J Hum Genet Año: 2015 Tipo del documento: Article País de afiliación: Países Bajos
Texto completo
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XML
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Proteínas Wnt / Proteína-6 Relacionada a Receptor de Lipoproteína de Baja Densidad / Exoma / Genes Dominantes / Anodoncia / Mutación Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Male Idioma: En Revista: Am J Hum Genet Año: 2015 Tipo del documento: Article País de afiliación: Países Bajos