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Sporadic COL4A1 mutations with extensive prenatal porencephaly resembling hydranencephaly.

Neurology - 1 Mar 2011

Meuwissen M E C, de Vries L S, Verbeek H A, Lequin M H, Govaert P P, Schot R, Cowan F M, Hennekam R, Rizzu P, Verheijen F W, Wessels M W, Mancini G M S

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Share to Cerebellar Diseases
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 21357838
DOI: 10.1212/WNL.0b013e31820e7751

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Sporadic COL4A1 mutations with extensive prenatal porencephaly resembling hydranencephaly.PMID 21357838Read ↗

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The expanding phenotype of COL4A1 and COL4A2 mutations: clinical data on 13 newly identified families and a review of the literature.Semantic proximity Read ↗

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COL4A1 mutations as a potential novel cause of autosomal dominant CAKUT in humansSemantic proximity Read ↗

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Infantile hemiparesis and porencephaly due to a COL4A1 mutation: Gould syndrome.Semantic proximity Read ↗

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