Pitfalls in restriction fragment length polymorphism analysis of Leber's hereditary optic neuropathy patients
Mitochondrion
.
2004 Jun;4(1):37-9.
doi: 10.1016/j.mito.2004.05.003.
Authors
F Carrara
1
,
P F Chinnery
,
P Yu-Wai-Man
,
M Zeviani
,
V Tiranti
Affiliation
1
Unit 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.
PMID:
16120372
DOI:
10.1016/j.mito.2004.05.003
No abstract available