TY  - GEN
AU  - Shimazaki,H
AU  - Takiyama,Y
AU  - Sakoe,K
AU  - Ikeguchi,K
AU  - Niijima,K
AU  - Kaneko,J
AU  - Namekawa,M
AU  - Ogawa,T
AU  - Date,H
AU  - Tsuji,S
AU  - Nakano,I
AU  - Nishizawa,M
TI  - Early-onset ataxia with ocular motor apraxia and hypoalbuminemia: the aprataxin gene mutations
SN  - 0028-3878
PY  - 2002///0920
KW  - Adult
KW  - Age of Onset
KW  - Apraxias
KW  - diagnosis
KW  - Brain
KW  - diagnostic imaging
KW  - Cerebellum
KW  - pathology
KW  - Chromosomes, Human, Pair 9
KW  - genetics
KW  - Comorbidity
KW  - DNA Mutational Analysis
KW  - DNA-Binding Proteins
KW  - Disease Progression
KW  - Female
KW  - Hematologic Diseases
KW  - Humans
KW  - Japan
KW  - epidemiology
KW  - Magnetic Resonance Imaging
KW  - Male
KW  - Middle Aged
KW  - Mutation
KW  - Nuclear Proteins
KW  - Oculomotor Muscles
KW  - physiopathology
KW  - Pedigree
KW  - Serum Albumin
KW  - deficiency
KW  - Spinocerebellar Degenerations
KW  - Sural Nerve
KW  - Tomography, X-Ray Computed
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1212/wnl.59.4.590
ER  -