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Article

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

Acta neuropathologica - 1 Nov 2007

Hinttala Reetta, Karttunen Vesa, Karttunen Ari, Herva Riitta, Uusimaa Johanna, Remes Anne M

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 17805552
DOI: 10.1007/s00401-007-0292-8

Genes

GFAP

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

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Research trail→

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Alexander disease with occipital predominance and a novel c.799G>C mutation in the GFAP gene.PMID 17805552Read ↗

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

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

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

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

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

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

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

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Alexander Disease: A Literature Review for Clinicians.Semantic proximity Read ↗

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