Primary pathogenic mtDNA mutations in multigeneration pedigrees with Leber hereditary optic neuropathy [5]

American Journal of Human Genetics

Volumn 59, Issue 2, 1996, Pages 481-485

  Mackey, D A ^a   Oostra, R J ^a   Rosenberg, T ^a   Nikoskelainen, E ^a   Bronte Stewart, J ^a   Poulton, J ^a   Harding, A E ^a   Govan, G ^a   Bolhuis, P A ^a   Norby, S ^a   Bleeker Wagemakers, E M ^a   Savontaus, M L ^a   Chan, C ^a   Howell, N ^a  

^a University of Texas Medical Branch School of Medicine   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL DNA; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE DEHYDROGENASE (UBIQUINONE);

AMINO ACID SUBSTITUTION; EXTRACHROMOSOMAL INHERITANCE; FEMALE; GENE MUTATION; HEREDITARY OPTIC ATROPHY; HUMAN; LETTER; MAJOR CLINICAL STUDY; MALE; MITOCHONDRION; PEDIGREE; PRIORITY JOURNAL;

AUSTRALIA; DNA, MITOCHONDRIAL; EUROPE; FEMALE; HUMANS; MALE; MODELS, GENETIC; MUTATION; NEW ZEALAND; OPTIC ATROPHIES, HEREDITARY; PEDIGREE;

EID: 0029816017     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter

References (0)