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Exome sequencing identifies INPPL1 mutations as a cause of opsismodysplasia
scientific article
Author/s
author: Valérie Cormier-Daire, Martine Le Merrer, Arnold Munnich, Andrea Superti-Furga, Anne-Lise Delezoide, Christine Bôle-Feysot, Patrick Nitschké, Celine Huber, Deborah Bartholdi, Joelle Roume
Work details
Publication date
January 10, 2013
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Language
English
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