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Latest research by NII scientists raises new hope for mitochondrial disorders

In the new study, the researchers at National Institute of Immunology focused on autosomal dominant progressive external ophthalmoplegia (adPEO) as it is one of the most common Mitochondrial disorders......................

Father of a rare disease child patient appeals for govt’s attention

New Delhi based Praveen Tyagi's son Garvit was detected with rare genetic disorder, Spinal Muscular Atrophy that has only one treatment option that cures the disease by only 40 percent. He has sought health ministry's help...