NLM Catalog
Indexing
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- Predictors of Obstructive Sleep Apnea Risk among Blacks with Metabolic Syndrome
- Molecular Mechanism Linking BRCA1 Dysfunction to High Grade Serous Epithelial Ovarian Cancers with Peritoneal Permeability and Ascites
- Objectively Coding Intervention Fidelity During A Phone-Based Obesity Prevention Study
- Acculturation and Subclinical Atherosclerosis among U.S. South Asians: Findings from the MASALA study
- Wake-up Strokes Are Similar to Known-Onset Morning Strokes in Severity and Outcome
- Endothelial Cells May Have Tissue-Specific Origins
Prion Diseases
Prion diseases, a group of disorders caused by abnormally shaped proteins called prions, occur in sporadic (Jakob-Creutzfeldt disease), genetic (genetic Jakob-Creutzfeldt disease, Gerstmann-Stra¨ussler-Scheinker syndrome.
Gene-targeting pharmaceuticals for single gene disorders
The concept of orphan drugs for treatment of orphan genetic diseases is perceived enthusiastically at present, and this is leading to research investment on the part of governments, disease-specific foundations, and industry.
Molecular diagnostic experience of whole-exome sequencing in adult patients
Whole-exome sequencing (WES) is increasingly used as a diagnostic tool in medicine, but prior reports focus on predominantly pediatric cohorts with neurologic or developmental disorders.
A novel intranuclear RNA vector system for long-term stem cell modification
Genetically modified stem and progenitor cells have emerged as a promising regenerative platform in the treatment of genetic and degenerative disorders, highlighted by their successful therapeutic use in inherent immunodeficiencies.
Genome-wide Association Studies Identify Genetic Loci Associated with Albuminuria in Diabetes
Elevated concentrations of albumin in the urine, albuminuria, are a hallmark of diabetic kidney disease and associate with increased risk for end-stage renal disease and cardiovascular events.
INDEXING
ABSTRACTING
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Journal of Genetic Mutation Disorders
Journal of Genetic Mutation Disorders (JGMD) is an international open access, peer-reviewed journal for the publication of advancements and for dissemination of scientific knowledge on Genetic mutation disorders by covering all aspects like Gene therapy, hereditary genetic disorders, Medical Genetics, Clinical Genetics etc., making it to be visible for various researchers.
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Online Submission System
Journal of Genetic Mutation Disorders is using online manuscript submission, review and tracking systems for quality and quick review processing. Review processing is performed by the editorial board members of Journal of Genetic Mutation Disorders or outside experts; at least two independent reviewer's approval followed by editor approval is required for acceptance of any citable manuscript.
