Earlier this week, a team of researchers announced that they’d made a discovery about how we inherit mitochondrial dna from ...

DNA study reveals crocs that lived in the Seychelles represented the westernmost population of saltwater crocodiles, having ...

A research team has successfully demonstrated the world's first gene-editing treatment for Leber's hereditary optic ...

EMA recommends Kygevvi for rare thymidine kinase 2 deficiency. It is the first authorized treatment for this disease.

A genetic analysis of the Deep Maniots living in Greece's southern Peloponnese region has revealed a close-knit, patriarchal ...

A research team led by Professor Hyunji Lee of the Department of Convergence Medicine at Korea University College of Medicine (co-first authors: PhD candidates Sanghun Kim, Ji Eun Kim, and Sungjin Ju; ...

The EMA’s positive opinion on Kygevvi marks a turning point for patients with TK2d, an ultra-rare genetic muscle disease previously managed only with supportive care.

Highlights advancing clinical-stage pipeline, including two major value-creating programs for primary immunodeficiencies ...

Over time, Crocodylus porosus achieved one of the widest ranges among reptiles. Before extinction in Seychelles, the species ...

A new genetic study has revealed that the people of Deep Mani, who inhabit one of the remotest regions of mainland Greece, ...

Established in 2017, National Missing Persons Day occurs annually on February 3 as a way to raise awareness for those who are missing.

Highlights advancing clinical-stage pipeline, including two major value-creating programs for primary immunodeficiencies (PIDs) with immune dysregulation and mtDNA-driven mitochondrial diseaseIntroduc ...