TY  - GEN
AU  - Méneret,Aurélie
AU  - Ahmar-Beaugendre,Yara
AU  - Rieunier,Guillaume
AU  - Mahlaoui,Nizar
AU  - Gaymard,Bertrand
AU  - Apartis,Emmanuelle
AU  - Tranchant,Christine
AU  - Rivaud-Péchoux,Sophie
AU  - Degos,Bertrand
AU  - Benyahia,Baya
AU  - Suarez,Felipe
AU  - Maisonobe,Thierry
AU  - Koenig,Michel
AU  - Durr,Alexandra
AU  - Stern,Marc-Henri
AU  - Dubois d'Enghien,Catherine
AU  - Fischer,Alain
AU  - Vidailhet,Marie
AU  - Stoppa-Lyonnet,Dominique
AU  - Grabli,David
AU  - Anheim,Mathieu
TI  - The pleiotropic movement disorders phenotype of adult ataxia-telangiectasia
SN  - 1526-632X
PY  - 2014///1224
KW  - Adult
KW  - Age of Onset
KW  - Ataxia Telangiectasia
KW  - epidemiology
KW  - Ataxia Telangiectasia Mutated Proteins
KW  - genetics
KW  - Chromosomal Instability
KW  - Cohort Studies
KW  - Disease Progression
KW  - Dysarthria
KW  - Dystonia
KW  - Eye Movement Measurements
KW  - Female
KW  - Genetic Pleiotropy
KW  - Humans
KW  - Immunoglobulins
KW  - deficiency
KW  - Male
KW  - Mobility Limitation
KW  - Movement Disorders
KW  - Mutation, Missense
KW  - Myoclonus
KW  - Ocular Motility Disorders
KW  - Phenotype
KW  - Severity of Illness Index
KW  - Young Adult
KW  - alpha-Fetoproteins
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1212/WNL.0000000000000794
ER  -