Clinical Genetics and Novel Therapies of Genetic Diseases
Thalassemia is a hereditary issue which is caused because of unusual haemoglobin creation. Thalassemia is hereditary sickness acquired from an individual's father and mother. There are most significant sort, alpha thalassemia and beta thalassemia. The seriousness of alpha and beta thalassemia depends upon on how among the four qualities for alpha globin or two qualities for beta globin is inadequate.
- Signs and symptoms
- Pathophysiology
- Management of thalassemia
Related Conference of Clinical Genetics and Novel Therapies of Genetic Diseases
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Clinical Genetics and Novel Therapies of Genetic Diseases Conference Speakers
Recommended Sessions
- Bioinformatics, Machine learning and Statistical methods
- Cancer, Cardiovascular Diseases and Genetics
- Clinical Genetics and Novel Therapies of Genetic Diseases
- Epigenetics and Gene Regulation
- Evolutionary and Population Genetics
- Functional Genomics and Transcriptomics
- Gene Cloning and Mapping
- Human Genetics
- Molecular and Cytogenetics
- Molecular Effects of Genetic Variation
- Molecular Phenotyping and Omics Technologies
- Mutation Detection and Analysis
- Pharmacogenomics
- Sickle cell Anaemia Genomics
- Stem cell Transplantation
- Translational Medicine
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