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SGCE Rabbit Pab
2021 Code Changes Reference Guide
Supplemental Table 1. List of Candidate Gene Filters Used in the Analysis of Exome Sequencing. MYOPATHY NEUROPATHY MND ABHD5
Neuromuscular Disorders
Genetic Testing Medical Policy – Genetics
The Effect of Mechanical Force on Gene Expression of Human Bladder Smooth Muscle Cells" (2012)
ISPD Mutations Account for a Small Proportion of Italian Limb Girdle Muscular Dystrophy Cases
Alteration of Striatal Dopaminergic Neurotransmission in a Mouse Model of DYT11 Myoclonus-Dystonia
HALOPLEX DISEASE RESEARCH PANELS Premium Performance with Content You Can Trust
Quantitative Proteomic Comparison of Myofibroblasts Derived from Bone
Please Find the Updated Gene List Here
Proteomic Profiling of the Interface Between the Stomach Wall and The
Limb-Girdle Muscle Weakness
Factors Regulating the Function and Assembly of the Sarcoglycan Complex in Brain
The Role of Delta Sarcoglycan in Dystrophin-Glycoprotein Complex Function in Cardiac Muscle
After a Review of the Current Available Literature, CGS Administrators Has Determined That Testing for the Following Genes/Gene
Genetic Heterogeneity in Ten Families with Myoclonus-Dystonia
Top View
Gene Table of Monogenic Neuromuscular Disorders (Nuclear Genome Only) Vol
Transcriptomic Profile of Primary Culture of Skeletal Muscle Cells
Coping with Cold: an Integrative, Multitissue Analysis of the Transcriptome of a Poikilothermic Vertebrate
Supplemental Materials Detailed Methods Mice. C57BL/6J Wild Type
Myoclonus-Dystonia (DYT11, DYT-SGCE) — a Channelopathy?
SGCE Gene Sarcoglycan Epsilon
Functional and Molecular Properties of DYT-SGCE Myoclonus-Dystonia Patient-Derived Striatal Medium Spiny Neurons
Adeno-Associated Virus Mediated Β-Sarcoglycan Gene Replacement Therapy for the Treatment of Limb Girdle Muscular Dystrophy Type 2E
Myoclonus-Dystonia and Ε-Sarcoglycan — Neurodevelopment, Channel, and Signaling Dysfunction
The Glomerular Transcriptome and a Predicted Protein–Protein Interaction Network
HALOPLEX DISEASE RESEARCH PANELS Premium Performance with Content You Can Trust
Technology Assessment
Duchenne Muscular Dystrophy
Test Catalogue August 2020 Table of Contents CENTOGENE CLINICAL DIAGNOSTIC PRODUCTS and SERVICES
The Landscape of Genomic Imprinting at the Porcine SGCE/PEG10 Locus
EGL Test Description
Case Reports Hereditary Myoclonus Dystonia: a Novel SGCE Variant and Phenotype Including Intellectual Disability
Mutated in Myoclonus-Dystonia Syndrome, Is Maternally Imprinted