TY  - GEN
AU  - MANCHESTER,P T
AU  - CALHOUN,F P
TI  - Dominant hereditary optic atrophy with bitemporal field defects
SN  - 0096-6339
PY  - 2000///0701
KW  - Disease
KW  - Eye
KW  - Hemianopsia
KW  - Humans
KW  - Optic Atrophy, Autosomal Dominant
KW  - Optic Nerve
KW  - Optic Nerve Diseases
N1  - Publication Type: Journal Article
UR  - https://doi.org/10.1001/archopht.1958.00940080497021
ER  -