Human Mutations in NDE1 Cause Extreme Microcephaly with Lissencephaly-Reference-Cited by-同舟云学术

Human Mutations in NDE1 Cause Extreme Microcephaly with Lissencephaly

Published:2011-05 Issue:5 Volume:88 Page:536-547
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Alkuraya Fowzan S.,Cai Xuyu,Emery Carina,Mochida Ganeshwaran H.,Al-Dosari Mohammed S.,Felie Jillian M.,Hill R. Sean,Barry Brenda J.,Partlow Jennifer N.,Gascon Generoso G.,Kentab Amal,Jan Mohammad,Shaheen Ranad,Feng Yuanyi,Walsh Christopher A.

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference38 articles.

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3. Lissencephaly. A human brain malformation associated with deletion of the LIS1 gene located at chromosome 17p13;Dobyns;JAMA,1993

4. Doublecortin, a brain-specific gene mutated in human X-linked lissencephaly and double cortex syndrome, encodes a putative signaling protein;Gleeson;Cell,1998

5. Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations;Hong;Nat. Genet.,2000

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