Allelic association and deletions in autosomal recessive proximal spinal muscular atrophy: association of marker genotype with disease severity and candidate cDNAs.

Wirth, B; Hahnen, E; Morgan, K; DiDonato, C J; Dadze, A; Rudnik-Schöneborn, S; Simard, L R; Zerres, K; Burghes, A H

Wirth, B; Hahnen, E; Morgan, K; DiDonato, C J; Dadze, A; Rudnik-Schöneborn, S; Simard, L R; Zerres, K; Burghes, A H.

Affiliation

Wirth B; Institute of Human Genetics, Bonn, Germany.

Hum Mol Genet ; 4(8): 1273-84, 1995 Aug.

Article in En | MEDLINE | ID: mdl-7581364

Subject(s)

Alleles; DNA, Complementary/genetics; Gene Deletion; Muscular Dystrophies/genetics; Spinal Cord Diseases/genetics; Chromosomes, Human, Pair 5/genetics; Female; Genes, Recessive; Genetic Markers; Genotype; Haplotypes; Heterozygote; Humans; Male; Models, Genetic; Muscular Dystrophies/classification; Pedigree; Phenotype; Spinal Cord Diseases/classification

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Collection: 01-internacional Database: MEDLINE Main subject: Spinal Cord Diseases / Gene Deletion / DNA, Complementary / Alleles / Muscular Dystrophies Type of study: Risk_factors_studies Limits: Female / Humans / Male Language: En Journal: Hum Mol Genet Journal subject: BIOLOGIA MOLECULAR / GENETICA MEDICA Year: 1995 Type: Article Affiliation country: Germany

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