Frequent DNA variant in exon 2a of the survival motor neuron gene (SMN): a further possibility for distinguishing the two copies of the gene.

Hahnen, E T; Wirth, B

Hahnen, E T; Wirth, B.

Affiliation

Hahnen ET; Institute of Human Genetics, Bonn, Germany.

Hum Genet ; 98(1): 122-3, 1996 Jul.

Article in En | MEDLINE | ID: mdl-8682499

Subject(s)

Muscular Atrophy, Spinal/genetics; Mutation; Nerve Tissue Proteins/genetics; Polymorphism, Single-Stranded Conformational; Base Sequence; Cyclic AMP Response Element-Binding Protein; DNA Primers; Exons/genetics; Female; Humans; Male; Molecular Sequence Data; Pedigree; Polymerase Chain Reaction; RNA-Binding Proteins; SMN Complex Proteins

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Collection: 01-internacional Database: MEDLINE Main subject: Muscular Atrophy, Spinal / Polymorphism, Single-Stranded Conformational / Mutation / Nerve Tissue Proteins Limits: Female / Humans / Male Language: En Journal: Hum Genet Year: 1996 Type: Article Affiliation country: Germany

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