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

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.

Affiliation

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 de En | MEDLINE | ID: mdl-26387593

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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Protéines de type Wingless / Protéine-6 apparentée au récepteur des LDL / Exome / Gènes dominants / Anodontie / Mutation Type d'étude: Observational_studies / Prognostic_studies / Risk_factors_studies Limites: Female / Humans / Male Langue: En Journal: Am J Hum Genet Année: 2015 Type de document: Article Pays d'affiliation: Pays-Bas

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