Genetics of hemophilia: Why mutations matter more than ever in diagnosis and treatment

Genetics of hemophilia: Why mutations matter more than ever in diagnosis and treatment

Hemophilia, a rare inherited bleeding disorder, is primarily caused by mutations in specific genes that impair the body’s ability to produce clotting factors, leading to excessive bleeding and long-term complications. These mutations not only determine the severity of the disease but also shape its inheritance patterns across generations.

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