Disease relevance of the so-called secondary Leber hereditary optic neuropathy mutations [3]

American Journal of Human Genetics

Volumn 60, Issue 6, 1997, Pages 1539-1542

  Hofmann, S ^a   Bezold, R ^a   Jaksch, M ^a   Kaufhold, P ^a   Obermaier Kusser, B ^a   Gerbitz, K D ^a  

^a Klinikum Schwabing   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

CYTOCHROME B;

EXTRACHROMOSOMAL INHERITANCE; GENE ISOLATION; GENE MUTATION; HUMAN; HUMAN CELL; HUMAN TISSUE; LEBER CONGENITAL AMAUROSIS; LETTER; OPTIC NERVE DISEASE; PATHOGENICITY; PENETRANCE; PRIORITY JOURNAL;

EID: 0030985186     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1016/s0002-9297(07)64248-7     Document Type: Letter

References (14)

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