Farid Ullah

Mitochondria: It is all about energy

Structure, Function, and Pharmacology of Glutamate Receptor Ion Channels

A recessive variant in TFAM causes mtDNA depletion associated with primary ovarian insufficiency, seizures, intellectual disability and hearing loss

Homozygous GRID2 missense mutation predicts a shift in the D-serine binding domain of GluD2 in a case with generalized brain atrophy and unusual clinical features