MindMap Gallery Molecular basis of human genetic diseases
The molecular basis of human genetic diseases focuses on disease inheritance patterns, genetic testing and diagnosis, and the pathophysiology of genetic disorders. Inheritance patterns encompass autosomal dominant, autosomal recessive, X-linked, and mitochondrial inheritance. Genetic testing and diagnosis involve techniques such as PCR, sequencing, and microarray analysis, along with the interpretation of results. The pathophysiology of genetic disorders includes mechanisms leading to disease, such as gene mutations, epigenetic changes, and gene-environment interactions.
Edited at 2024-12-25 01:59:00