An inherited TUBB2B mutation alters a kinesin-binding site and causes polymicrogyria, CFEOM and axon dysinnervation-Reference-Cited by-同舟云学术

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

Published:2012-09-21 Issue:26 Volume:21 Page:5484-5499
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Cederquist Gustav Y.,Luchniak Anna,Tischfield Max A.,Peeva Maya,Song Yuyu,Menezes Manoj P.,Chan Wai-Man,Andrews Caroline,Chew Sheena,Jamieson Robyn V.,Gomes Lavier,Flaherty Maree,Grant Patricia Ellen,Gupta Mohan L.,Engle Elizabeth C.

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/21/26/5484/17257724/dds393.pdf

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5. During Drosophila spermatogenesis beta 1, beta 2 and beta 3 tubulin isotypes are cell-type specifically expressed but have the potential to coassemble into the axoneme of transgenic flies;Kaltschmidt;Eur. J. Cell. Biol.,1991

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