Detection of gene deletion in patients of Duchenne muscular dystrophy/Becker muscular dystrophy using polymerase chain reaction.

dc.contributor.authorSinha, Sen_US
dc.contributor.authorPradhan, Sen_US
dc.contributor.authorMittal, R Den_US
dc.contributor.authorMittal, Ben_US
dc.date.accessioned1992-10-01en_US
dc.date.accessioned2009-05-27T06:29:39Z
dc.date.available1992-10-01en_US
dc.date.available2009-05-27T06:29:39Z
dc.date.issued1992-10-01en_US
dc.description.abstractPolymerase chain reaction (PCR) was used to study the presence of gene deletion (the most prominent type of mutations) in some families afflicted by Duchenne muscular dystrophy/Becker muscular dystrophy (DMD/BMD). The results clearly demonstrate deletion in the central part of the DMD gene in two of the three families studied. This information can be useful for genetic counselling with particular reference to prenatal diagnosis and carrier analysis.en_US
dc.description.affiliationDepartment of Genetics, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow.en_US
dc.identifier.citationSinha S, Pradhan S, Mittal RD, Mittal B. Detection of gene deletion in patients of Duchenne muscular dystrophy/Becker muscular dystrophy using polymerase chain reaction. Indian Journal of Medical Research. 1992 Oct; 96(): 297-301en_US
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/16507
dc.language.isoengen_US
dc.source.urihttps://icmr.nic.in/ijmr/ijmr.htmen_US
dc.subject.meshBase Sequenceen_US
dc.subject.meshGene Deletionen_US
dc.subject.meshHumansen_US
dc.subject.meshMolecular Sequence Dataen_US
dc.subject.meshMuscular Dystrophies --blooden_US
dc.subject.meshPolymerase Chain Reactionen_US
dc.titleDetection of gene deletion in patients of Duchenne muscular dystrophy/Becker muscular dystrophy using polymerase chain reaction.en_US
dc.typeComparative Studyen_US
dc.typeJournal Articleen_US
dc.typeResearch Support, Non-U.S. Gov'ten_US
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