The <i>GBA</i> p.Trp378Gly mutation is a probable French‐Canadian founder mutation causing Gaucher disease and synucleinopathies
- DOI
- 10.1111/cge.13405
- Published
- 2018-07-16
- Container
- Clinical Genetics
- Publisher
- Wiley
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1111/cge.13405,
title = {The
<i>GBA</i>
p.Trp378Gly mutation is a probable French‐Canadian founder mutation causing Gaucher disease and synucleinopathies},
author = {J.A. Ruskey and S. Zhou and R. Santiago and L.‐A. Franche and A. Alam and L. Roncière and D. Spiegelman and E.A. Fon and J.‐F. Trempe and L.V. Kalia and R.B. Postuma and N. Dupre and G.‐E. Rivard and S. Assouline and D. Amato and Z. Gan‐Or},
year = {2018},
journal = {Clinical Genetics},
doi = {10.1111/cge.13405},
url = {https://doi.org/10.1111/cge.13405}
}RIS
TY - JOUR
TI - The
<i>GBA</i>
p.Trp378Gly mutation is a probable French‐Canadian founder mutation causing Gaucher disease and synucleinopathies
AU - J.A. Ruskey
AU - S. Zhou
AU - R. Santiago
AU - L.‐A. Franche
AU - A. Alam
AU - L. Roncière
AU - D. Spiegelman
AU - E.A. Fon
AU - J.‐F. Trempe
AU - L.V. Kalia
AU - R.B. Postuma
AU - N. Dupre
AU - G.‐E. Rivard
AU - S. Assouline
AU - D. Amato
AU - Z. Gan‐Or
PY - 2018
JO - Clinical Genetics
DO - 10.1111/cge.13405
UR - https://doi.org/10.1111/cge.13405
ER - APA
Ruskey, J., Zhou, S., Santiago, R., Franche, L., Alam, A., Roncière, L., Spiegelman, D., Fon, E., Trempe, J., Kalia, L., Postuma, R., Dupre, N., Rivard, G., Assouline, S., Amato, D., & Gan‐Or, Z. (2018). The <i>GBA</i> p.Trp378Gly mutation is a probable French‐Canadian founder mutation causing Gaucher disease and synucleinopathies. Clinical Genetics. https://doi.org/10.1111/cge.13405
Source records
- crossref · retrieved 2026-09-26T18:27:04.076Z