Development of genotypic diagnosis of Duchenne muscular dystrophy by multiplex PCR in Oran: A study of 5 cases of western Algeria

Development of genotypic diagnosis of Duchenne muscular dystrophy by multiplex PCR in Oran: A study of 5 cases of western Algeria

Duchenne Muscular Dystrophy (DMD) is the most common and severe form of muscular dystrophy, reaching one out of every 5000 male births in the world population. It is characterized by progressive muscular degeneration from a young age and leads to serious failures of the body which lead to the death...

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Bibliographic Details
Main Authors: Houssam BOULENOUAR, Fatima-Zohra MOGHTIT, Amine MELLOUK, Khaldia BENLHADJ-DJELLOUL, Hadjira OUHAIBI DJELLOULI, Mohamed BENMANSOUR, Sarah LARJAM HETRAF, Faouzia ZEMANI FODIL, Nadhira SAIDI MEHTAR, Sounnia MEDIENE BENCHEKOR
Format: Article
Language:English
Published: University of Oran 1 2022-04-01
Series:Journal de la Faculté de Médecine d'Oran
Subjects:
Duchenne musculardystrophy
Dystrophin
Multiplex PCR
deletions
X chromosome
Online Access:https://confajol3.ajol.info/index.php/jmfo/article/view/456

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