A new mtDNA mutation associated with Leber hereditary optic neuroretinopathy

American Journal of Human Genetics

Volumn 48, Issue 6, 1991, Pages 1147-1153

  Huoponen, K ^a   Vilkki, J ^a   Aula, P ^a   Nikoskelainen, E K ^a   Savontaus, M L ^a  

^a UNIVERSITY OF TURKU   (Finland)

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL DNA; NUCLEOTIDE;

AMINO ACID SUBSTITUTION; ARTICLE; CLINICAL ARTICLE; FEMALE; HEREDITARY OPTIC ATROPHY; HUMAN; MALE; MUTATION; NUCLEIC ACID BASE SUBSTITUTION; NUCLEOTIDE SEQUENCE; PEDIGREE; PRIORITY JOURNAL;

ANIMAL; BASE SEQUENCE; BLOTTING, SOUTHERN; DNA; DNA, MITOCHONDRIAL; FINLAND; HUMAN; MOLECULAR SEQUENCE DATA; MUTATION; OLIGONUCLEOTIDE PROBES; OPTIC ATROPHIES, HEREDITARY; PEDIGREE; POLYMERASE CHAIN REACTION; POLYMORPHISM, RESTRICTION FRAGMENT LENGTH; SEQUENCE ALIGNMENT; SEQUENCE HOMOLOGY, NUCLEIC ACID; SPECIES SPECIFICITY; SUPPORT, NON-U.S. GOV'T;

EID: 0025910614     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (0)