TY  - GEN
AU  - Chang,Chi-Wu
AU  - Chang,Chi-Huang
AU  - Peng,Mei-Lin
TI  - Leber's hereditary opric neuropathy: a case report
SN  - 1607-551X
PY  - 2004///0106
KW  - Child
KW  - DNA, Mitochondrial
KW  - genetics
KW  - Humans
KW  - Male
KW  - Optic Atrophy, Hereditary, Leber
KW  - Point Mutation
N1  - Publication Type: Case Reports; Journal Article
UR  - https://doi.org/10.1016/s1607-551x(09)70500-5
ER  -