Reevaluation of the linkage of an optic atrophy susceptibility gene to X- chromosomal markers in Finnish families with Leber hereditary optic neuroretinopathy (LHON) [2]

American Journal of Human Genetics

Volumn 53, Issue 1, 1993, Pages 289-292

  Juvonen, V ^a   Vilkki, J ^a   Aula, P ^a   Nikoskelainen, E ^a   Savontaus, M L ^a  

^a UNIVERSITY OF TURKU   (Finland)

Author keywords

[No Author keywords available]

Indexed keywords

CHROMOSOME MARKER; DISEASE PREDISPOSITION; GENETIC LINKAGE; HEREDITARY OPTIC ATROPHY; LETTER; OPTIC NERVE ATROPHY; PRIORITY JOURNAL; X CHROMOSOME LINKAGE;

ADULT; DNA, MITOCHONDRIAL; FEMALE; FINLAND; GENETIC MARKERS; GENETIC PREDISPOSITION TO DISEASE; HUMAN; LINKAGE (GENETICS); MALE; MIDDLE AGE; MONOAMINE OXIDASE; OPTIC ATROPHIES, HEREDITARY; PEDIGREE; POINT MUTATION; SUPPORT, U.S. GOV'T, P.H.S.; X CHROMOSOME;

EID: 0027483762     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter

References (0)