Clinical, biomarker, and molecular delineations and genotype-phenotype correlations of ataxia with oculomotor apraxia type 1

M Renaud, MC Moreira, BB Monga… - JAMA …, 2018 - jamanetwork.com
Importance Ataxia with oculomotor apraxia type 1 (AOA1) is an autosomal recessive
cerebellar ataxia due to mutations in the aprataxin gene (APTX) that is characterized by …
被引用次数：31 相关文章

Clinical, Biomarker, and Molecular Delineations and Genotype-Phenotype Correlations of Ataxia With Oculomotor Apraxia Type 1

M Renaud, MC Moreira, BB Monga, D Rodriguez… - JAMA …, 2018 - hcl.hal.science
Importance: Ataxia with oculomotor apraxia type 1 (AOA1) is an autosomal recessive
cerebellar ataxia due to mutations in the aprataxin gene (APTX) that is characterized by …

[引用][C] Clinical, Biomarker, and Molecular Delineations and Genotype-Phenotype Correlations of Ataxia With Oculomotor Apraxia Type 1

M Renaud, MC Moreira, BB Monga, D Rodriguez… - JAMA …, 2018 - cir.nii.ac.jp
Clinical, Biomarker, and Molecular Delineations and Genotype-Phenotype Correlations of
Ataxia With Oculomotor Apraxia Type 1 | CiNii Research CiNii 国立情報学研究所 学術情報 …

Clinical, Biomarker, and Molecular Delineations and Genotype-Phenotype Correlations of Ataxia With Oculomotor Apraxia Type 1

M Renaud, MC Moreira, F Ochsner, HH Jung - JAMA Neurology, 2018 - zora.uzh.ch
Importance Ataxia with oculomotor apraxia type 1 (AOA1) is an autosomal recessive
cerebellar ataxia due to mutations in the aprataxin gene (APTX) that is characterized by …

Clinical, Biomarker, and Molecular Delineations and Genotype-Phenotype Correlations of Ataxia With Oculomotor Apraxia Type 1

M Renaud, MC Moreira, BB Monga, D Rodriguez… - JAMA neurology, 2018 - hal.utc.fr
Importance: Ataxia with oculomotor apraxia type 1 (AOA1) is an autosomal recessive
cerebellar ataxia due to mutations in the aprataxin gene (APTX) that is characterized by …

Clinical, Biomarker, and Molecular Delineations and Genotype-Phenotype Correlations of Ataxia With Oculomotor Apraxia Type 1

M Renaud, MC Moreira, BB Monga… - JAMA …, 2018 - pubmed.ncbi.nlm.nih.gov
Importance Ataxia with oculomotor apraxia type 1 (AOA1) is an autosomal recessive
cerebellar ataxia due to mutations in the aprataxin gene (APTX) that is characterized by …

Clinical, Biomarker, and Molecular Delineations and Genotype-Phenotype Correlations of Ataxia With Oculomotor Apraxia Type 1.

M Renaud, MC Moreira, B Ben Monga… - JAMA …, 2018 - search.ebscohost.com
This study defines the clinical, biomarker, and molecular spectrum and provides genotype-
phenotype correlations among patients with ataxia with oculomotor apraxia type 1 from 18 …

Clinical, Biomarker, and Molecular Delineations and Genotype-Phenotype Correlations of Ataxia With Oculomotor Apraxia Type 1

M Renaud, MC Moreira, BB Monga… - JAMA …, 2018 - hal-obspm.ccsd.cnrs.fr
Importance: Ataxia with oculomotor apraxia type 1 (AOA1) is an autosomal recessive
cerebellar ataxia due to mutations in the aprataxin gene (APTX) that is characterized by …

Clinical, Biomarker, and Molecular Delineations and Genotype-Phenotype Correlations of Ataxia With Oculomotor Apraxia Type 1.

M Renaud, MC Moreira, B Monga, D Rodriguez… - JAMA …, 2018 - europepmc.org
Clinical, Biomarker, and Molecular Delineations and Genotype-Phenotype Correlations of
Ataxia With Oculomotor Apraxia Type 1. - Abstract - Europe PMC Sign in | Create an account …

Clinical, Biomarker, and Molecular Delineations and Genotype-Phenotype Correlations of Ataxia With Oculomotor Apraxia Type 1

M Renaud, MC Moreira, BB Monga… - JAMA …, 2018 - hal.parisnanterre.fr
Importance: Ataxia with oculomotor apraxia type 1 (AOA1) is an autosomal recessive
cerebellar ataxia due to mutations in the aprataxin gene (APTX) that is characterized by …