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Article

Linkage of a commoner form of recessive amyotrophic lateral sclerosis to chromosome 15q15-q22 markers

1 Dec 1998

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Share to Amyotrophic Lateral Sclerosis Research
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 9933301
DOI: 10.1007/s100480050052

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Related research

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Research trail→

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Linkage of a commoner form of recessive amyotrophic lateral sclerosis to chromosome 15q15-q22 markersPMID 9933301Read ↗

Two Families with Familial Amyotrophic Lateral Sclerosis Are Linked to a Novel Locus on Chromosome 16qSemantic proximity Read ↗

Linkage of recessive familial amyotrophic lateral sclerosis to chromosome 2q33–q35Semantic proximity Read ↗

Linkage of autosomal recessive hereditary spastic paraplegia with mental impairment and thin corpus callosum to chromosome 15A13-15.Semantic proximity Read ↗

Identification of Two Novel Loci for Dominantly Inherited Familial Amyotrophic Lateral SclerosisSemantic proximity Read ↗

Linkage of a Gene Causing Familial Amyotrophic Lateral Sclerosis to Chromosome 21 and Evidence of Genetic-Locus HeterogeneitySemantic proximity Read ↗

SPG15, a new locus for autosomal recessive complicated HSP on chromosome 14q.Semantic proximity Read ↗

Linkage of Familial Amyotrophic Lateral Sclerosis With Frontotemporal Dementia to Chromosome 9q21-q22Semantic proximity Read ↗

A novel locus for late onset amyotrophic lateral sclerosis/motor neurone disease variant at 20q13Semantic proximity Read ↗

Autosomal dominant familial spastic paraplegia: tight linkage to chromosome 15q.Semantic proximity Read ↗

Preferential localization of the limb-girdle muscular dystrophy type 2A gene in the proximal part of a 1-cM 15q15.1-q15.3 interval.Semantic proximity Read ↗

Identification of 2 Loci at chromosomes 9 and 14 in a multiplex family with frontotemporal lobar degeneration and amyotrophic lateral sclerosis.Semantic proximity Read ↗

A gene for autosomal recessive limb-girdle muscular dystrophy maps to chromosome 2p.Semantic proximity Read ↗

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