Loss-of-Function Mutations in the WNT Co-receptor LRP6 Cause Autosomal-Dominant Oligodontia-Reference-Cited by-同舟云学术

Loss-of-Function Mutations in the WNT Co-receptor LRP6 Cause Autosomal-Dominant Oligodontia

Published:2015-10 Issue:4 Volume:97 Page:621-626
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

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

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

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