Mitochondrial complex III deficiency associated with a homozygous mutation in UQCRQ Ortal Barel Laboratory of Dr. Ohad Birk Ben Gurion University Beer-Sheva,
Mutations in Lamin A are the Cause of Hutchinson-Gilford Progeria Syndrome Francis S. Collins, M.D., Ph.D. July 28, 2003.
Mitochondrial complex III deficiency associated with a homozygous mutation in UQCRQ Ortal Barel
