First clinical and genetic analysis of LRRK2 G2019S, R1441G/C/H/, I2020T and Y1699C mutations in Costa Rican patients with Parkinson's disease
Publication
, Conference
Hernandez-Guillen, A; Lobo-Prada, T; Ruiz-Martinez, J; Gorostidi-Pagola, A; Gan-Or, Z; Carazo-Cespedes, K; Fornaguera-Trias, J; Torrealba-Acosta, G
Published in: MOVEMENT DISORDERS
2020
Duke Scholars
Published In
MOVEMENT DISORDERS
EISSN
1531-8257
ISSN
0885-3185
Publication Date
2020
Volume
35
Start / End Page
S198 / S198
Related Subject Headings
- Neurology & Neurosurgery
- 3209 Neurosciences
- 3202 Clinical sciences
- 1109 Neurosciences
- 1106 Human Movement and Sports Sciences
- 1103 Clinical Sciences
Citation
APA
Chicago
ICMJE
MLA
NLM
Hernandez-Guillen, A., Lobo-Prada, T., Ruiz-Martinez, J., Gorostidi-Pagola, A., Gan-Or, Z., Carazo-Cespedes, K., … Torrealba-Acosta, G. (2020). First clinical and genetic analysis of LRRK2 G2019S, R1441G/C/H/, I2020T and Y1699C mutations in Costa Rican patients with Parkinson's disease. In MOVEMENT DISORDERS (Vol. 35, pp. S198–S198).
Hernandez-Guillen, A., T. Lobo-Prada, J. Ruiz-Martinez, A. Gorostidi-Pagola, Z. Gan-Or, K. Carazo-Cespedes, J. Fornaguera-Trias, and G. Torrealba-Acosta. “First clinical and genetic analysis of LRRK2 G2019S, R1441G/C/H/, I2020T and Y1699C mutations in Costa Rican patients with Parkinson's disease.” In MOVEMENT DISORDERS, 35:S198–S198, 2020.
Hernandez-Guillen A, Lobo-Prada T, Ruiz-Martinez J, Gorostidi-Pagola A, Gan-Or Z, Carazo-Cespedes K, et al. First clinical and genetic analysis of LRRK2 G2019S, R1441G/C/H/, I2020T and Y1699C mutations in Costa Rican patients with Parkinson's disease. In: MOVEMENT DISORDERS. 2020. p. S198–S198.
Hernandez-Guillen, A., et al. “First clinical and genetic analysis of LRRK2 G2019S, R1441G/C/H/, I2020T and Y1699C mutations in Costa Rican patients with Parkinson's disease.” MOVEMENT DISORDERS, vol. 35, 2020, pp. S198–S198.
Hernandez-Guillen A, Lobo-Prada T, Ruiz-Martinez J, Gorostidi-Pagola A, Gan-Or Z, Carazo-Cespedes K, Fornaguera-Trias J, Torrealba-Acosta G. First clinical and genetic analysis of LRRK2 G2019S, R1441G/C/H/, I2020T and Y1699C mutations in Costa Rican patients with Parkinson's disease. MOVEMENT DISORDERS. 2020. p. S198–S198.
Published In
MOVEMENT DISORDERS
EISSN
1531-8257
ISSN
0885-3185
Publication Date
2020
Volume
35
Start / End Page
S198 / S198
Related Subject Headings
- Neurology & Neurosurgery
- 3209 Neurosciences
- 3202 Clinical sciences
- 1109 Neurosciences
- 1106 Human Movement and Sports Sciences
- 1103 Clinical Sciences