Evidence against an X-linked visual loss susceptibility locus in Leber hereditary optic neuropathy

American Journal of Human Genetics

Volumn 59, Issue 1, 1996, Pages 103-108

  Chalmers, R M ^a   Davis, M B ^a   Sweeney, M G ^a   Wood, N W ^a   Harding, A E ^a  

^a UNIVERSITY COLLEGE LONDON   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL DNA;

ADULT; ARTICLE; CLINICAL ARTICLE; CONTROLLED STUDY; FAMILY; FEMALE; GENE LOCUS; GENE MUTATION; GENETIC LINKAGE; GENETIC SUSCEPTIBILITY; HEREDITARY OPTIC ATROPHY; HUMAN; HUMAN CELL; ITALY; MALE; PEDIGREE ANALYSIS; PENETRANCE; PRIORITY JOURNAL; UNITED KINGDOM; VISUAL IMPAIRMENT; X CHROMOSOME INACTIVATION; X CHROMOSOME LINKAGE;

DNA, MITOCHONDRIAL; DOSAGE COMPENSATION, GENETIC; FEMALE; GENETIC MARKERS; GREAT BRITAIN; HUMANS; LINKAGE (GENETICS); LOD SCORE; MALE; MODELS, GENETIC; OPTIC ATROPHIES, HEREDITARY; PEDIGREE; POLYMORPHISM, GENETIC; X CHROMOSOME;

EID: 0029981001     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (0)