γ-sarcoglycan and dystrophin mutation spectrum in an Algerian cohort.

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γ-sarcoglycan and dystrophin mutation spectrum in an Algerian cohort.

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2016 nî lūn-bûn

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2016年の論文

@ja

2016年論文

@yue

2016年論文

@zh-hant

2016年論文

@zh-hk

2016年論文

@zh-mo

2016年論文

@zh-tw

2016年论文

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2016年论文

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2016年论文

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name

γ-sarcoglycan and dystrophin mutation spectrum in an Algerian cohort.

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γ-sarcoglycan and dystrophin mutation spectrum in an Algerian cohort.

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prefLabel

γ-sarcoglycan and dystrophin mutation spectrum in an Algerian cohort.

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P1476

γ-sarcoglycan and dystrophin mutation spectrum in an Algerian cohort.

@en

P2093

Abdelmadjid Hamri

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Carinne Roudaut

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Imene Dalichaouche

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Isabelle Richard

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Karima Sifi

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Leila Rouabah

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Noureddine Abadi

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P2860

Deletion screening of the Duchenne muscular dystrophy locus via multiplex DNA amplification

Analysis of Dystrophin Gene Deletions by Multiplex PCR in Moroccan Patients

A simple salting out procedure for extracting DNA from human nucleated cells

Mutations that disrupt the carboxyl-terminus of gamma-sarcoglycan cause muscular dystrophy

Dystrophin: the protein product of the Duchenne muscular dystrophy locus

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

Novel sarcoglycan gene mutations in a large cohort of Italian patients.

Carrier frequency of the c.525delT mutation in the SGCG gene and estimated prevalence of limb girdle muscular dystrophy type 2C among the Moroccan population.

Detection of 98% of DMD/BMD gene deletions by polymerase chain reaction.

An explanation for the phenotypic differences between patients bearing partial deletions of the DMD locus.

P304

129-135

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P31

scholarly article

P356

10.1002/MUS.25443

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P433

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P478

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P50

Yamina Sifi

P577

2016-10-19T00:00:00Z

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P698

27759885

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P921

Algeria