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PMID: 3398004 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Partial gene duplication in Duchenne and Becker muscular dystrophies.

Journal of medical genetics ·Vol. 25 ·No. 6 ·1988-06-00 ·Pages 369-76

Hu XY, Burghes AH, Ray PN, Thompson MW, Murphy EG, Worton RG

Abstract

Duchenne and Becker muscular dystrophies (DMD and BMD) are progressive muscle wasting disorders with an X linked recessive mode of inheritance. We have surveyed 120 unrelated patients with DMD or BMD for gene duplications using a series of genomic probes from within the DMD/BMD gene locus. In three patients, two with DMD and one with BMD, a duplicated region within the DMD/BMD locus has been shown by Southern blot analysis and transmission densitometry. In two cases a new restriction fragment spanning the duplication junction has been visualised, indicating that the duplications are tandemly arranged. Mendelian inheritance of the duplication has been shown in two families by following the segregation of the duplication junction fragment. The three duplication cases have been analysed with a cDNA probe isolated from the DXS206 region of the DMD/BMD locus and the duplication of a specific set of exons has been found in two cases. This study shows that all three duplications are internal to the gene and confirms that such a duplication can result in a genetic disorder through the disruption of exon organisation.

MeSH Terms
Child Humans Male Multigene Family Muscular Dystrophies/genetics
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Hu X Y
Genetics Department, Hospital for Sick Children, Toronto, Canada.
Burghes A H
Ray P N
Thompson M W
Murphy E G
Worton R G
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Article Info
Journal
Journal of medical genetics
Abbr.
J Med Genet
ISSN
0022-2593
Published
1988-06-00
Pages
369-76
Language
English
Region
England
NLM ID
2985087R
PMCID
PMC1050503
Subset
IM
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