Pitfalls in restriction fragment length polymorphism analysis of Leber's hereditary optic neuropathy patients

F Carrara1, P F Chinnery, P Yu-Wai-Man

  • 1Unit of Molecular Neurogenetics--Pierfranco and Luisa Mariani Center for the Study of Mitochondrial Disorders in Children, National Neurological Institute C. Besta, Via Temolo 4, 20126 Milan, Italy.

Mitochondrion
|August 27, 2005
PubMed
Abstract

No abstract available in PubMed .

Related Concept Videos