TY  - GEN
AU  - Le Ber,Isabelle
AU  - Bouslam,Naïma
AU  - Rivaud-Péchoux,Sophie
AU  - Guimarães,João
AU  - Benomar,Ali
AU  - Chamayou,Céline
AU  - Goizet,Cyril
AU  - Moreira,Maria-Ceù
AU  - Klur,Sandra
AU  - Yahyaoui,Mohamed
AU  - Agid,Yves
AU  - Koenig,Michel
AU  - Stevanin,Giovanni
AU  - Brice,Alexis
AU  - Dürr,Alexandra
TI  - Frequency and phenotypic spectrum of ataxia with oculomotor apraxia 2: a clinical and genetic study in 18 patients
SN  - 0006-8950
PY  - 2004///0520
KW  - Adolescent
KW  - Adult
KW  - Age of Onset
KW  - Apraxias
KW  - genetics
KW  - Biomarkers
KW  - blood
KW  - Child
KW  - Child, Preschool
KW  - Disease Progression
KW  - Gait Ataxia
KW  - Genetic Linkage
KW  - Haplotypes
KW  - Humans
KW  - Lod Score
KW  - Middle Aged
KW  - Neuropsychological Tests
KW  - Ocular Motility Disorders
KW  - Pedigree
KW  - Phenotype
KW  - alpha-Fetoproteins
KW  - analysis
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1093/brain/awh080
ER  -