Mutations inMYT1, encoding the myelin transcription factor 1, are a rare cause of OAVS-Reference-Cited by-同舟云学术

Mutations inMYT1, encoding the myelin transcription factor 1, are a rare cause of OAVS

Published:2016-06-29 Issue:11 Volume:53 Page:752-760
ISSN:0022-2593
Container-title:Journal of Medical Genetics
language:en
Short-container-title:J Med Genet

Author:

Lopez Estelle,Berenguer Marie,Tingaud-Sequeira Angèle,Marlin Sandrine,Toutain Annick,Denoyelle Françoise,Picard Arnaud,Charron Sabine,Mathieu Guilaine,de Belvalet Harmony,Arveiler Benoit,Babin Patrick J,Lacombe Didier,Rooryck Caroline

Publisher

BMJ

Subject

Genetics (clinical),Genetics

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