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GDAP1
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Analysis of Gene Expression in the Nervous System Identifies Key Genes and Novel Candidates for Health and Disease
A Genomic Approach to Delineating the Occurrence of Scoliosis in Arthrogryposis Multiplex Congenita
Some Bioinformatic Analyses of Human GDAP1 Gene Expression
Case Report: Exome Sequencing Achieved a Definite Diagnosis in A
A Yeast-Based Model for Hereditary Motor and Sensory Neuropathies: a Simple System for Complex, Heterogeneous Diseases
One Multilocus Genomic Variation Is Responsible for a Severe Charcot–Marie–Tooth Axonal Form
SUPPLEMENTARY MATERIAL Sanger Sequencing the Coding
Mutation Frequency for Charcot-Marie-Tooth Disease Type 1
Genetics of Charcot-Marie-Tooth Disease Type 4A: Mutations
Molecular Diagnosis of Hereditary Neuropathies by Whole Exome Sequencing and Expanding the Phenotype Spectrum
Novel Compound Heterozygous Missense Mutations in GDAP1 Cause Charcot–Marie–Tooth Type 4A
GDAP1 Involvement in Mitochondrial Function and Oxidative Stress, Investigated in a Charcot-Marie-Tooth Model of Hipscs-Derived Motor Neurons
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Analysis of Gene Expression in the Nervous System Identifies Key
Gene Ontology Analysis of Arthrogryposis (Multiple Congenital Contractures)
Identification of Candidate Genes Associated with Charcot-Marie- Tooth Disease by Network and Pathway Analysis
Peripheral Neuropathy in Mitochondrial Disorders
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YY1-Dependent Transcriptional Regulation of the Human GDAP1 Gene
Product Description SALSA® MLPA® Probemix P353-B1 CMT4 to Be Used with the MLPA General Protocol
Detecting Gene Modules Differentially Expressed in Multiple Human Brain
Analysis of Gene Expression in the Nervous System Identifies Key Genes and Novel Candidates for Health and Disease
Supplemental Information Complement Protein C1q Directs
S42003-019-0513-4.Pdf
Finding the Causes of Inherited Neuropathies
Mutations in the LMNA Gene Do Not Cause Axonal CMT in Czech Patients
Molecular Genetics of Autosomal-Dominant Axonal Charcot-Marie-Tooth Disease
Systematic Large-Scale Study of the Inheritance Mode of Mendelian Disorders Provides New Insight Into Human Diseasome