Clinical and genetic characteristics of type 3 lissencephaly caused by a mutation in the TUBA1A gene (OMIM: 611603)

Clinical and genetic characteristics of type 3 lissencephaly caused by a mutation in the TUBA1A gene (OMIM: 611603)

Background. Lissencephaly (LIS) is a spectrum of malformations of the cerebral cortex that occur as a result of impaired migration of neuronal precursors to the cortical plate and the formation of furrows and convolutions in the post‑migration period of embryonic development. In recent years, a sign...

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Bibliographic Details
Main Authors: D. M. Guseva, T. V. Markova, L. A. Bessonova, S. S. Nikitin, E. L. Dadali, O. A. Shchagina
Format: Article
Language:Russian
Published: ABV-press 2021-04-01
Series:Нервно-мышечные болезни
Subjects:
brain malformation
lissencephaly
microcephaly
tubulin
tuba1a
Online Access:https://nmb.abvpress.ru/jour/article/view/423
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