A homozygous founder mutation inTRAPPC6Bassociates with a neurodevelopmental disorder characterised by microcephaly, epilepsy and autistic features

Published 2017 View Full Article

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Title
A homozygous founder mutation inTRAPPC6Bassociates with a neurodevelopmental disorder characterised by microcephaly, epilepsy and autistic features
Authors
Keywords
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Journal
JOURNAL OF MEDICAL GENETICS
Volume 55, Issue 1, Pages 48-54
Publisher
BMJ
Online
2017-06-17
DOI
10.1136/jmedgenet-2017-104627

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