Journal of Genetic Syndromes & Gene Therapy

Journal of Genetic Syndromes & Gene Therapy
Open Access

ISSN: ISSN: 2157-7412

Volume 16, Issue 1 (2025)

Perspective

Pages: 1 - 0

Genomic Technologies and their Impact on Autosomal Recessive Disorders

Martine Clunie*

DOI: 10.35248/2157-7412.25.16.458

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Perspective

Pages: 1 - 2

The Role of UBE3A in Angelman Syndrome: Insights and Therapeutic Opportunities

Joseph Judson*

DOI: 10.35248/2157-7412.25.16.462

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Pages: 1 - 2

Targeting Inflammation in Huntington's Disease: Potential Therapeutic Strategies

Divyanka Trivedi*

DOI: 10.35248/2157-7412.25.16.461

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Pages: 1 - 0

Sickle Cell Disease and Its Complications: Focus on Acute Chest Syndrome

Miguel Nascimento*

DOI: 10.35248/2157-7412.25.16.460

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Opinion Article

Pages: 1 - 2

Ion Channel and Synaptic Gene Mutations in Epileptic Encephalopathies

Eloise Garnier*

DOI: 10.35248/2157-7412.25.16.444

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Pages: 1 - 2

Clinical Guidelines for the Diagnosis and Management of Hemoglobin E/Beta-Thalassemia

Phuong Le Vuong*

DOI: 10.35248/2157-7412.25.16.457

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Pages: 1 - 2

Gene Editing Technologies in Somatic Gene Therapy: Innovations and Challenges

Milena Adera*

DOI: 10.35248/2157-7412.25.16.456

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Short Communication

Pages: 1 - 2

Recent Advances in Diagnosis of Down Syndrome Using Molecular Techniques

Harper Westwood*

DOI: 10.35248/2157-7412.25.16.453

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Pages: 1 - 2

CRISPR-Cas9: Transforming Biotechnology in Agriculture Enhancing Crop Durability in Changing Climates

Honghao Li* and Limei Wei

DOI: 10.35248/2157-7412.25.16.454

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Opinion Article

Pages: 1 - 2

Role of HTT Gene Mutations in Huntington's Disease Pathogenesis and Therapy Development

Mateus Rocha*

DOI: 10.35248/2157-7412.25.16.445

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Opinion Article

Pages: 1 - 2

Molecular Mechanisms and Therapeutic Prospects in Rett Syndrome

Johann Meier*

DOI: 10.35248/2157-7412.25.16.446

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Commentary

Pages: 1 - 2

Comparative Genomic Studies in Angelman and Prader-Willi Syndromes

Liang Xuemin*

DOI: 10.35248/2157-7412.25.16.447

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Perspective

Pages: 1 - 2

Multisystem Involvement in Turner Syndrome: Genetic and Clinical Aspects

Beatrice Holloway*

DOI: 10.35248/2157-7412.25.16.448

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Pages: 1 - 2

Genotype-Phenotype Correlations in Fragile X Syndrome

Nikolay Petrov*

DOI: 10.35248/2157-7412.25.16.449

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Perspective

Pages: 1 - 2

Genetic Heterogeneity and Clinical Variability in Noonan Syndrome

Camila Restrepo*

DOI: 10.35248/2157-7412.25.16.450

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Commentary

Pages: 1 - 2

Neurodevelopmental Features and Genomic Analysis of Williams Syndrome

Rohan Deshmukh*

DOI: 10.35248/2157-7412.25.16.451

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Commentary

Pages: 1 - 2

Role of FBN1 Mutations in the Pathogenesis of Marfan Syndrome

Liesbeth Wilde*

DOI: 10.35248/2157-7412.25.16.452

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