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Molecular analysis among a group of Egyptian Duchenne muscular dystrophy patients using real-time PCR

Abstract

Background
Duchenne muscular dystrophy (DMD) is a neuromuscular disease of children caused by dystrophin protein deficiency encoded by dystrophin gene that is localized to the short arm of the X chromosome, position 21.1q. dystrophin gene mutation results in this disorder. Dystrophin is necessary for keeping the integrity of both skeletal and smooth muscles.
Aim
Identify...
Keywords
Exon
Duchenne muscular dystrophy
Dystrophin
Outpatient clinic
Muscular dystrophy
Medicine
Genetics
Biology
Genotype
Mutation
Group A
Gene
Molecular biology
Internal medicine
Sustainable Development Goals (SDG)
Good health and well-being



Molecular analysis among a group of Egyptian Duchenne muscular dystrophy patients using real-time PCR

Molecular analysis among a group of Egyptian Duchenne muscular dystrophy patients using real-time PCR

Abstract

Background
Duchenne muscular dystrophy (DMD) is a neuromuscular disease of children caused by dystrophin protein deficiency encoded by dystrophin gene that is localized to the short arm of the X chromosome, position 21.1q. dystrophin gene mutation results in this disorder. Dystrophin is necessary for keeping the integrity of both skeletal and smooth muscles.
Aim
Identify...
Keywords
Exon
Duchenne muscular dystrophy
Dystrophin
Outpatient clinic
Muscular dystrophy
Medicine
Genetics
Biology
Genotype
Mutation
Group A
Gene
Molecular biology
Internal medicine
Sustainable Development Goals (SDG)
Good health and well-being