TY  - GEN
AU  - Schieving,J H
AU  - de Vries,B B A
AU  - Hol,F
AU  - Stroink,H
TI  - [Sudden blindness: consider Leber's hereditary optic neuropathy]
SN  - 0028-2162
PY  - 2008///1218
KW  - Blindness
KW  - etiology
KW  - Child
KW  - DNA, Mitochondrial
KW  - genetics
KW  - Diagnosis, Differential
KW  - Humans
KW  - Male
KW  - Mutation
KW  - Optic Atrophy, Hereditary, Leber
KW  - complications
KW  - Young Adult
N1  - Publication Type: Case Reports; English Abstract; Journal Article
ER  -