Distribution of dystrophin gene deletions in a Chinese population

DMD mutation spectrum analysis in 613 Chinese patients with dystrophinopathy

(2015) Ruolan Guo et al.   JOURNAL OF HUMAN GENETICS

Duchenne/Becker muscular dystrophy: A report on clinical, biochemical, and genetic study in Gujarat population, India

(2014) MandavaV Rao et al.   Annals of Indian Academy of Neurology

MLPA Application in Clinical Diagnosis of DMD/BMD in Shanghai

(2014) Xing Ji et al.   JOURNAL OF CLINICAL LABORATORY ANALYSIS

Sensitivity and Frequencies of Dystrophin Gene Mutations in Thai DMD/BMD Patients As Detected by Multiplex PCR

(2013) Thanyachai Sura et al.   DISEASE MARKERS

Exon Deletion Patterns of the Dystrophin Gene in 82 Vietnamese Duchenne/Becker Muscular Dystrophy Patients

(2013) Van Khanh Tran et al.   JOURNAL OF NEUROGENETICS

Genotype and phenotype characterization in a large dystrophinopathic cohort with extended follow-up

(2011) Francesca Magri et al.   JOURNAL OF NEUROLOGY

Combination of conventional multiplex PCR and quantitative real-time PCR detects large rearrangements in the dystrophin gene in 59% of Syrian DMD/BMD patients

(2010) Ammar Madania et al.   CLINICAL BIOCHEMISTRY

Mutation spectrum of the dystrophin gene in 442 Duchenne/Becker muscular dystrophy cases from one Japanese referral center

(2010) Yasuhiro Takeshima et al.   JOURNAL OF HUMAN GENETICS

Deletional mutations of dystrophin gene and carrier detection in eastern India

(2009) Jayasri Basak et al.   INDIAN JOURNAL OF PEDIATRICS

Mutation Analysis in a Population-Based Cohort of Boys With Duchenne or Becker Muscular Dystrophy

(2008) Christopher Cunniff et al.   JOURNAL OF CHILD NEUROLOGY

Intragenic deletions in the dystrophin gene in 211 Pakistani Duchenne muscular dystrophy patients

(2008) Muhammad J Hassan et al.   PEDIATRICS INTERNATIONAL