A novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar heterotopia and lissencephaly syndrome (Q24314944)

GOA release 2020-03-11

author

Cherif Beldjord

13

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Pierre Billuart

object named as

P Billuart

3

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author name string

V des Portes

1

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J M Pinard

2

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M C Vinet

4

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A Koulakoff

5

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A Carrié

6

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A Gelot

7

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E Dupuis

8

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J Motte

9

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Y Berwald-Netter

10

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M Catala

11

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A Kahn

12

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J Chelly

The agyria-pachygyria complex: a spectrum of cortical malformations.

14

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language of work or name

English

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publication date

9 January 1998

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published in

Cell

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volume

92

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issue

1

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page(s)

51-61

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cites work

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Dominant X linked subcortical laminar heterotopia and lissencephaly syndrome (XSCLH/LIS): evidence for the occurrence of mutation in males and mapping of a potential locus in Xq22

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X-linked malformations of neuronal migration

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Doublecortin, a brain-specific gene mutated in human X-linked lissencephaly and double cortex syndrome, encodes a putative signaling protein

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Miller-Dieker lissencephaly gene encodes a subunit of brain platelet-activating factor acetylhydrolase [corrected]

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Subcortical laminar heterotopia and lissencephaly in two families: a single X linked dominant gene.

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Linkage and physical mapping of X-linked lissencephaly/SBH (XLIS): a gene causing neuronal migration defects in human brain

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