Infantile neurodegenerative disorder associated with mutations in TBCD, an essential gene in the tubulin heterodimer assembly pathway

Infantile neurodegenerative disorder associated with mutations in TBCD, an essential gene in the tubulin heterodimer assembly pathway

© The Author 2016. Published by Oxford University Press. Mutation in a growing spectrum of genes is known to either cause or contribute to primary or secondary microcephaly. In primary microcephaly the genetic determinants frequently involve mutations that contribute to or modulate the microtubule c...

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Main Authors: Edvardson, S., Tian, G., Cullen, H., Vanyai, H., Ngo, L., Bhat, S., Aran, A., Daana, M., Da'amseh, N., Abu-Libdeh, B., Cowan, N., Heng, Julian, Elpeleg, O.
Format: Journal Article
Published: Oxford University Press 2016
Online Access:http://hdl.handle.net/20.500.11937/71955

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http://hdl.handle.net/20.500.11937/71955

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