Disruption of RAB40AL function leads to Martin–Probst syndrome, a rare X-linked multisystem neurodevelopmental human disorder

Title
Disruption of RAB40AL function leads to Martin–Probst syndrome, a rare X-linked multisystem neurodevelopmental human disorder
Authors
Keywords
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Journal
JOURNAL OF MEDICAL GENETICS
Volume 49, Issue 5, Pages 332-340
Publisher
BMJ
Online
2012-05-11
DOI
10.1136/jmedgenet-2011-100575

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