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Article

Neuropathological phenotype of a distinct form of lissencephaly associated with mutations in TUBA1A.

Brain : a journal of neurology - 1 Sept 2008

Fallet-Bianco Catherine, Loeuillet Laurence, Poirier Karine, Loget Philippe, Chapon Françoise, Pasquier Laurent, Saillour Yoann, Beldjord Cherif, Chelly Jamel, Francis Fiona

Abstract excerpt

Lissencephalies are congenital malformations responsible for epilepsy and mental retardation in children. A number of distinct lissencephaly syndromes have been characterized, according to the aspect and the topography of the cortical malformation, the involvement of other cerebral structures and...

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Identifiers

PMID: 18669490
DOI: 10.1093/brain/awn155

Genes

ARX
DCX
RELN

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-18669490-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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Neuropathological phenotype of a distinct form of lissencephaly associated with mutations in TUBA1A.PMID 18669490Read ↗

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