Mutation spectrum analysis of Duchenne/Becker muscular dystrophy in 68 families in Kuwait: The era of personalized medicine.

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Mutation spectrum analysis of Duchenne/Becker muscular dystrophy in 68 families in Kuwait: The era of personalized medicine.

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2018 nî lūn-bûn

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2018年学术文章

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2018年学术文章

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2018年学术文章

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name

Mutation spectrum analysis of ...... era of personalized medicine.

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Mutation spectrum analysis of ...... era of personalized medicine.

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Mutation spectrum analysis of ...... era of personalized medicine.

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Mutation spectrum analysis of ...... era of personalized medicine.

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Mutation spectrum analysis of ...... era of personalized medicine.

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Mutation spectrum analysis of ...... era of personalized medicine.

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P1476

Mutation spectrum analysis of ...... e era of personalized medicine

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Adel Baqer

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Alaa Elshafey

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Haya Al-Balool

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Hayat Alaboud

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Laila Bastaki

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Mohammed Al Ben Ali

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P2860

The importance of genetic diagnosis for Duchenne muscular dystrophy

Population frequencies of inherited neuromuscular diseases--a world survey

Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals

DMD Mutations in 576 Dystrophinopathy Families: A Step Forward in Genotype-Phenotype Correlations

Interaction of dystrophin rod domain with membrane phospholipids. Evidence of a close proximity between tryptophan residues and lipids.

Effects of systemic multiexon skipping with peptide-conjugated morpholinos in the heart of a dog model of Duchenne muscular dystrophy.

A convenient multiplex PCR system for the detection of dystrophin gene deletions: a comparative analysis with cDNA hybridisation shows mistypings by both methods.

Genetic diagnosis as a tool for personalized treatment of Duchenne muscular dystrophy.

Translation from a DMD exon 5 IRES results in a functional dystrophin isoform that attenuates dystrophinopathy in humans and mice.

Molecular diagnosis of duchenne muscular dystrophy: past, present and future in relation to implementing therapies

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e0197205

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scholarly article

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10.1371/JOURNAL.PONE.0197205

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English

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Fawziah Mohammed

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2018-05-30T00:00:00Z

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29847600

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5976149

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