Neuropathological Hallmarks of Brain Malformations in Extreme Phenotypes Related to DYNC1H1 Mutations-Reference-Cited by-同舟云学术

Neuropathological Hallmarks of Brain Malformations in Extreme Phenotypes Related to DYNC1H1 Mutations

Published:2017-03-10 Issue: Volume: Page:
ISSN:0022-3069
Container-title:Journal of Neuropathology & Experimental Neurology
language:en
Short-container-title:

Author:

Laquerriere Annie,Maillard Camille,Cavallin Mara,Chapon Françoise,Marguet Florent,Molin Arnaud,Sigaudy Sabine,Blouet Marie,Benoist Guillaume,Fernandez Carla,Poirier Karine,Chelly Jamel,Thomas Sophie,Bahi-Buisson Nadia

Publisher

Oxford University Press (OUP)

Subject

Cellular and Molecular Neuroscience,Neurology (clinical),Neurology,General Medicine,Pathology and Forensic Medicine

Link

http://academic.oup.com/jnen/article-pdf/76/3/195/11008377/nlw124.pdf

Reference37 articles.

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2. Mutations in tubulin genes are frequent causes of various foetal malformations of cortical development including microlissencephaly;Acta Neuropathol Commun,2014

3. Malformations of cortical development: clinical features and genetic causes;Lancet Neurol,2014

4. Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly;Nat Genet,2013

5. The wide spectrum of tubulinopathies: what are the key features for the diagnosis?;Brain,2014

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