An inherited TUBB2B mutation alters a kinesin-binding site and causes polymicrogyria, CFEOM and axon dysinnervation

Title
An inherited TUBB2B mutation alters a kinesin-binding site and causes polymicrogyria, CFEOM and axon dysinnervation
Authors
Keywords
-
Journal
HUMAN MOLECULAR GENETICS
Volume 21, Issue 26, Pages 5484-5499
Publisher
Oxford University Press (OUP)
Online
2012-09-22
DOI
10.1093/hmg/dds393

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