Area of research
Electrical and Electronic Engineering · Molecular Biology
Research interest
Research interests include Muscle Physiology and Disorders, Advanced MIMO Systems Optimization, Advanced Wireless Communication Techniques, and Genetic Neurodegenerative Diseases.
[Identification of a novel variant in a patient with Calsequestrin 1 related myopathy].
Gene analysis and clinical features of 22 GNE myopathy patients
The Clinical, Myopathological, and Genetic Analysis of 20 Patients With Non-dystrophic Myotonia
Genetic origin of patients having spastic paraplegia with or without other neurologic manifestations
Adolescent/adult-onset homocysteine remethylation disorders characterized by gait disturbance with/without psychiatric symptoms and cognitive decline: a series of seven cases
The clinical and genetic heterogeneity analysis of five families with primary periodic paralysis
A clinical, pathological and molecular biology features of 81 patients with myotonic myopathies
VCP myopathy: A family with unusual clinical manifestations
Clinical and Genetic Features of Patients with Juvenile Amyotrophic Lateral Sclerosis with Fused in Sarcoma (FUS) Mutation
Characterization and genetic diagnosis of centronuclear myopathies in seven Chinese patients
Neutral lipid storage disease with distal weakness: report of one family
Clinical, pathological and molecular biological study of six patients with collagen type VI related myopathies
MYH7 mutation associated with two phenotypes of myopathy
Identification of novel mutations of the<i>CLCN1</i>gene for myotonia congenital in China
Next generation sequencing reveals ryanodine receptor 1 mutations in a Chinese central core disease cohort
Cardiac effects of the c.1583 C→G LMNA mutation in two families with Emery-Dreifuss muscular dystrophy
Early myocardial damage assessment in dystrophinopathies using 99Tcm-MIBI gated myocardial perfusion imaging
Optimization PCR for Detection CTG/CCTG-Repeat Expansions in the Diagnosis of Myotonic Dystrophies.
PubMed 2015cited by 4position: middle
Clinical and genetic analyses of two female Duchenne muscular dystrophy manifesting carriers and their families
Clinical, Pathological, and Neuroimaging Analyses of Two Cases of Leigh Syndrome in a Chinese Family
Significance of phosphatidyl inositol 3-kinase expression in amyotrophic lateral sclerosis atrophy muscle fibers
An analysis of clinical features and pathology in 40 patients with dysferlinopathy
DYSF mutation analysis in a group of Chinese patients with dysferlinopathy