A MITOCHONDRIAL MUTATION AT NT-9101 IN THE ATP SYNTHASE-6 GENE ASSOCIATED WITH DEFICIENT OXIDATIVE-PHOSPHORYLATION IN A FAMILY WITH LEBER HEREDITARY OPTIC NEURORETINOPATHY

Authors
LAMMINEN T MAJANDER A JUVONEN V WIKSTROM M AULA P NIKOSKELAINEN E SAVONTAUS ML
Citation
T. Lamminen et al., A MITOCHONDRIAL MUTATION AT NT-9101 IN THE ATP SYNTHASE-6 GENE ASSOCIATED WITH DEFICIENT OXIDATIVE-PHOSPHORYLATION IN A FAMILY WITH LEBER HEREDITARY OPTIC NEURORETINOPATHY, American journal of human genetics, 56(5), 1995, pp. 1238-1240
Citations number
11
Categorie Soggetti
Genetics & Heredity
Journal title
American journal of human genetics → ACNP
ISSN journal
00029297
Volume
56
Issue
5
Year of publication
1995
Pages
1238 - 1240
Database
ISI
SICI code
0002-9297(1995)56:5<1238:AMMANI>2.0.ZU;2-3