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Article

A novel GFAP mutation in a type II (late-onset) Alexander disease patient.

Journal of neurology - 1 Apr 2016

de Paiva Anderson Rodrigues Brandão, Freua Fernando, Lucato Leandro Tavares, Parmera Jacy, Dória Denise, Nóbrega Paulo Ribeiro, Olávio Thiago Rosa, Macedo-Souza Lúcia Inês, Kok Fernando

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Identifiers

PMID: 26914930
DOI: 10.1007/s00415-016-8065-8

Genes

GFAP

Provenance

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Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

A novel GFAP mutation in a type II (late-onset) Alexander disease patient.PMID 26914930Read ↗

A novel mutation in the GFAP gene in a familial adult onset Alexander disease.Semantic proximity Read ↗

Type II (adult onset) Alexander disease in a paraplegic male with a rare D128N mutation in the GFAP gene.Semantic proximity Read ↗

Adult-onset Alexander disease with unusual inflammatory features and a novel GFAP mutation in two patients.Semantic proximity Read ↗

Adult Alexander disease with de novo c.1193C>T heterozygous variant in GFAP gene.Semantic proximity Read ↗

Alexander disease: GFAP mutations unify young and old.Semantic proximity Read ↗

Novel GFAP mutation in patient with adult-onset Alexander disease presenting with spastic ataxia.Semantic proximity Read ↗

Alexander disease with occipital predominance and a novel c.799G>C mutation in the GFAP gene.Semantic proximity Read ↗

Parkinsonism phenotype in a family with adult onset Alexander disease and a novel mutation of GFAP.Semantic proximity Read ↗

Authors' response to: "Alexander disease genetics: Beyond GFAP exon sequencing?"Semantic proximity Read ↗

A systematic review and meta-analysis of GFAP gene variants in Alexander disease.Semantic proximity Read ↗

Alexander disease genetics: Beyond GFAP exon sequencing?Semantic proximity Read ↗

Pathologic Alexander Disease with Normal GFAP Sequencing: An Autopsy Case Report and Literature Review.Semantic proximity Read ↗

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