Segregation of mitochondrial genomes in a heteroplasmic lineage with Leber hereditary optic neuroretinopathy

American Journal of Human Genetics

Volumn 47, Issue 1, 1990, Pages 95-100

  Vilkki, J ^a   Savontaus, M L ^a   Nikoskelainen, E K ^a  

^a UNIVERSITY OF TURKU   (Finland)

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL DNA;

ARTICLE; CASE REPORT; GENE STRUCTURE; GENETIC ENGINEERING; HEREDITARY OPTIC ATROPHY; HEREDITY; HUMAN; HUMAN CELL; MALE; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL;

BASE SEQUENCE; DNA, MITOCHONDRIAL; FEMALE; HEREDITARY MOTOR AND SENSORY NEUROPATHIES; HUMAN; MALE; MOLECULAR SEQUENCE DATA; OLIGONUCLEOTIDE PROBES; OPTIC ATROPHIES, HEREDITARY; PEDIGREE; POLYMORPHISM, RESTRICTION FRAGMENT LENGTH; SUPPORT, NON-U.S. GOV'T;

EID: 0025375332     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (0)