Exome sequencing identifies INPPL1 mutations as a cause of opsismodysplasia.
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A. Munnich | C. Bole-Feysot | P. Nitschké | J. Roume | E. Faqeih | D. Cavalcanti | D. Bartholdi | V. Cormier-Daire | A. Superti-Furga | S. Shalev | M. le Merrer | C. Huber | Z. Borochowitz | A. Delezoide | H. Santos | A. Frigo | C. Bôle-Feysot