Is gene deletion in eukaryotes sequence-dependent? A study of nine deletion junctions and nineteen other deletion breakpoints in intron 7 of the human dystrophin gene.

McNaughton, J C; Cockburn, D J; Hughes, G; Jones, W A; Laing, N G; Ray, P N; Stockwell, P A; Petersen, G B

McNaughton, J C; Cockburn, D J; Hughes, G; Jones, W A; Laing, N G; Ray, P N; Stockwell, P A; Petersen, G B.

Affiliation

McNaughton JC; Department of Biochemistry and Centre for Gene Research, University of Otago, P.O. Box 56, Dunedin, New Zealand.

Gene ; 222(1): 41-51, 1998 Nov 05.

Article in En | MEDLINE | ID: mdl-9813236

Subject(s)

Dystrophin/genetics; Gene Deletion; Introns; Muscular Dystrophies/genetics; Base Sequence; Chromosome Breakage; Cloning, Molecular; Cluster Analysis; Eukaryotic Cells; Humans; Models, Genetic; Molecular Sequence Data; Polymerase Chain Reaction; Recombination, Genetic; Sequence Analysis, DNA

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Collection: 01-internacional Database: MEDLINE Main subject: Introns / Dystrophin / Gene Deletion / Muscular Dystrophies Type of study: Prognostic_studies Limits: Humans Language: En Journal: Gene Year: 1998 Document type: Article Affiliation country: New Zealand

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