Detection of the mtDNA 14484 mutation on an African-specific haplotype: Implications about its role in causing leber hereditary optic neuropathy [1]

American Journal of Human Genetics

Volumn 59, Issue 1, 1996, Pages 248-252

  Torroni, A ^a   Carelli, V ^a   Petrozzi, M ^a   Terracina, M ^a   Barboni, P ^a   Malpassi, P ^a   Wallace, D C ^a   Scozzari, R ^a  

^a SAPIENZA UNIVERSITY OF ROME   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL DNA;

ADULT; CASE REPORT; HAPLOTYPE; HEREDITARY OPTIC ATROPHY; HUMAN; LETTER; MALE; MISSENSE MUTATION; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; TUNISIA;

ADULT; AFRICA; DNA, MITOCHONDRIAL; EVOLUTION, MOLECULAR; FEMALE; HAPLOTYPES; HUMANS; MALE; MUTATION; OPTIC ATROPHIES, HEREDITARY;

EID: 0029895877     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter

References (0)