(Q51950786)
Statements
A double mutation (G11778A and G12192A) in mitochondrial DNA associated with Leber's hereditary optic neuropathy and cardiomyopathy. (English)
1 reference
Masakazu Mimaki
1 reference
Akemi Ikota
1 reference
Aya Sato
1 reference
Hirofumi Komaki
1 reference
Jun Akanuma
1 reference
Ikuya Nonaka
1 reference
Yu-ichi Goto
1 reference
1 January 2003
1 reference
48
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1
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47-50
1 reference
Identifiers
1 reference