This is the peer reviewed version of the following article: [Ruskey, J.A., Zhou, S., Santiago, R., Franche, L.-A., Alam, A., Roncière, L., Spiegelman, D., Fon, E.A., Trempe, J.-F., Kalia, L.V., et al. (2018). TheGBAp.Trp378Gly mutation is a probable French-Canadian founder mutation causing Gaucher disease and synucleinopathies. Clinical Genetics 94, 339–345.], which has been published in final form at https://doi.org/10.1111/cge.13405. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions. Deposited by shareyourpaper.org and openaccessbutton.org. We've taken reasonable steps to ensure this content doesn't violate copyright. However, if you think it does you can r...
This is the peer reviewed version of the following article: Caimari, F. , Kumar, A. V., Kurzawinski,...
Background: Gaucher disease (GD) is the most frequent lysosomal storage disorder; type 1 is by far t...
Pallido-pyramidal syndromes combine dystonia with or without parkinsonism and spasticity as part of ...
This is the peer reviewed version of the following article: [Gan‐Or, Z., Alcalay, R.N., Makarious, M...
European Neighbourhood Policy covering the Mediterranean Partner Countries[Article in French]Gaucher...
Copyright © 2015 A. Mesut Erzurumluoglu et al. This is an open access article distributed under the ...
Gaucher disease, the most prevalent lysosomal storage disease, results from an inherited deficiency ...
Gaucher disease, the most prevalent lysosomal storage disease characterized by a remarkable degree o...
This is the peer reviewed version of the following article: [Gan-Or, Z., Yoon, G., Suchowersky, O., ...
First published: 11 July 2016Abstract not availableChristopher P. Barnett, Nathalie J. Nataren, Manu...
ABSTRACT: The characterization of the underlying GALC gene lesions was performed in 30 unrelated pat...
[[abstract]]Gaucher disease, the most prevalent lysosomal storage disease characterized by a remarka...
Contains fulltext : 47801.pdf (publisher's version ) (Closed access)Missense mutat...
[Objectives]: Gaucher disease (GD) is the most common inherited lysosomal storage disease, caused by...
GBA variants carriers are at increased risk of Parkinson's disease (PD) and Lewy body dementia (LBD)...
This is the peer reviewed version of the following article: Caimari, F. , Kumar, A. V., Kurzawinski,...
Background: Gaucher disease (GD) is the most frequent lysosomal storage disorder; type 1 is by far t...
Pallido-pyramidal syndromes combine dystonia with or without parkinsonism and spasticity as part of ...
This is the peer reviewed version of the following article: [Gan‐Or, Z., Alcalay, R.N., Makarious, M...
European Neighbourhood Policy covering the Mediterranean Partner Countries[Article in French]Gaucher...
Copyright © 2015 A. Mesut Erzurumluoglu et al. This is an open access article distributed under the ...
Gaucher disease, the most prevalent lysosomal storage disease, results from an inherited deficiency ...
Gaucher disease, the most prevalent lysosomal storage disease characterized by a remarkable degree o...
This is the peer reviewed version of the following article: [Gan-Or, Z., Yoon, G., Suchowersky, O., ...
First published: 11 July 2016Abstract not availableChristopher P. Barnett, Nathalie J. Nataren, Manu...
ABSTRACT: The characterization of the underlying GALC gene lesions was performed in 30 unrelated pat...
[[abstract]]Gaucher disease, the most prevalent lysosomal storage disease characterized by a remarka...
Contains fulltext : 47801.pdf (publisher's version ) (Closed access)Missense mutat...
[Objectives]: Gaucher disease (GD) is the most common inherited lysosomal storage disease, caused by...
GBA variants carriers are at increased risk of Parkinson's disease (PD) and Lewy body dementia (LBD)...
This is the peer reviewed version of the following article: Caimari, F. , Kumar, A. V., Kurzawinski,...
Background: Gaucher disease (GD) is the most frequent lysosomal storage disorder; type 1 is by far t...
Pallido-pyramidal syndromes combine dystonia with or without parkinsonism and spasticity as part of ...