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Exome sequencing identifies INPPL1 mutations as a cause of opsismodysplasia

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Description scientific article
Author/s

author: Deborah Bartholdi  Patrick Nitschké  Martine Le Merrer  Christine Bôle-Feysot  Valérie Cormier-Daire  Andrea Superti-Furga  Anne-Lise Delezoide  Celine Huber  Joelle Roume  Arnold Munnich 

Publication date January 10, 2013
Language English
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