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Volume 12, Issue 2 (2023)

Commentary

Genetic Variations and Disease Susceptibility: Insights from Human Immunology

DOI: 10.35248/2161-1041.23.12.251

Opinion

Targeting DNA Damage Pathways as Therapeutic Strategies in Rheumatoid Arthritis

DOI: 10.35248/2161-1041.23.12.242

Commentary

Variations in Symptomatology and Disease Progression: The Role of Hereditary Alpha-Tryptasemia in Congenital Hypermobility Disorders (CHDs)

DOI: 10.35248/2161-1041.23.12.243

Commentary

Decoding the Genetic Complexity of Hereditary Bleeding and Platelet Disorders using Next-Generation Sequencing

DOI: 10.35248/2161-1041.23.12.244

Opinion

Obligate and Manifesting Carriers: The Complexities of X-Linked Inherited Retinal Diseases

DOI: 10.35248/2161-1041.23.12.245

Perspective

Innovative Strategies for Liver Cancer: Ribozyme-Mediated RNA Replacement

DOI: 10.35248/2161-1041.23.12.246

Short Communication

Enhancing Diagnostic Accuracy: The Significance of RNA Analysis in Hereditary Cancer Testing

DOI: 10.35248/2161-1041.23.12.247

Perspective

Long-term Care and Support: The Ongoing Role of Genetic Counseling in Inherited Heart Conditions

DOI: 10.35248/2161-1041.23.12.248

Perspective

Functional Implications of Disease-Associated Variants: Insights from Population Genetics

DOI: 10.35248/2161-1041.23.12.249

Perspective

Novel Therapeutic Approaches: Insights from Genetic Research in Non syndromic Congenital Hearing Loss

DOI: 10.35248/2161-1041.23.12.250