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Mutation in the SYNJ1 gene associated with autosomal recessive, early-onset Parkinsonism. / Quadri, Marialuisa; Fang, Mingyan; Picillo, Marina; Olgiati, Simone; Breedveld, Guido J.; Graafland, Josja; Wu, Bin; Xu, Fengping; Erro, Roberto; Amboni, Marianna; Pappata, Sabina; Quarantelli, Mario; Annesi, Grazia; Quattrone, Aldo; Chien, Hsin F.; Barbosa, Egberto R.; Oostra, Ben A.; Barone, Paolo; Wang, Jun; Bonifati, Vincenzo.
In:
Human Mutation, Vol. 34, No. 9, 2013, p. 1208-1215.
Research output: Contribution to journal › Journal article › Research › peer-review
Harvard
Quadri, M, Fang, M, Picillo, M, Olgiati, S, Breedveld, GJ, Graafland, J, Wu, B, Xu, F, Erro, R, Amboni, M, Pappata, S, Quarantelli, M, Annesi, G, Quattrone, A, Chien, HF, Barbosa, ER, Oostra, BA, Barone, P, Wang, J & Bonifati, V 2013, '
Mutation in the SYNJ1 gene associated with autosomal recessive, early-onset Parkinsonism',
Human Mutation, vol. 34, no. 9, pp. 1208-1215.
https://doi.org/10.1002/humu.22373APA
Quadri, M., Fang, M., Picillo, M., Olgiati, S., Breedveld, G. J., Graafland, J., Wu, B., Xu, F., Erro, R., Amboni, M., Pappata, S., Quarantelli, M., Annesi, G., Quattrone, A., Chien, H. F., Barbosa, E. R., Oostra, B. A., Barone, P., Wang, J., & Bonifati, V. (2013).
Mutation in the SYNJ1 gene associated with autosomal recessive, early-onset Parkinsonism.
Human Mutation,
34(9), 1208-1215.
https://doi.org/10.1002/humu.22373Vancouver
Quadri M, Fang M, Picillo M, Olgiati S, Breedveld GJ, Graafland J et al.
Mutation in the SYNJ1 gene associated with autosomal recessive, early-onset Parkinsonism.
Human Mutation. 2013;34(9):1208-1215.
https://doi.org/10.1002/humu.22373Author
Quadri, Marialuisa ; Fang, Mingyan ; Picillo, Marina ; Olgiati, Simone ; Breedveld, Guido J. ; Graafland, Josja ; Wu, Bin ; Xu, Fengping ; Erro, Roberto ; Amboni, Marianna ; Pappata, Sabina ; Quarantelli, Mario ; Annesi, Grazia ; Quattrone, Aldo ; Chien, Hsin F. ; Barbosa, Egberto R. ; Oostra, Ben A. ; Barone, Paolo ; Wang, Jun ; Bonifati, Vincenzo. / Mutation in the SYNJ1 gene associated with autosomal recessive, early-onset Parkinsonism. In: Human Mutation. 2013 ; Vol. 34, No. 9. pp. 1208-1215.
Bibtex
@article{c31206b8c4c44abe97de53ef0d7c0c26,
title = "Mutation in the SYNJ1 gene associated with autosomal recessive, early-onset Parkinsonism",
keywords = "Parkinsonism, dystonia, dementia, SYNJ1, PINK1, gene, mutation",
author = "Marialuisa Quadri and Mingyan Fang and Marina Picillo and Simone Olgiati and Breedveld, {Guido J.} and Josja Graafland and Bin Wu and Fengping Xu and Roberto Erro and Marianna Amboni and Sabina Pappata and Mario Quarantelli and Grazia Annesi and Aldo Quattrone and Chien, {Hsin F.} and Barbosa, {Egberto R.} and Oostra, {Ben A.} and Paolo Barone and Jun Wang and Vincenzo Bonifati",
year = "2013",
doi = "10.1002/humu.22373",
language = "English",
volume = "34",
pages = "1208--1215",
journal = "Human Mutation",
issn = "1059-7794",
publisher = "JohnWiley & Sons, Inc.",
number = "9",
}
RIS
TY - JOUR
T1 - Mutation in the SYNJ1 gene associated with autosomal recessive, early-onset Parkinsonism
AU - Quadri, Marialuisa
AU - Fang, Mingyan
AU - Picillo, Marina
AU - Olgiati, Simone
AU - Breedveld, Guido J.
AU - Graafland, Josja
AU - Wu, Bin
AU - Xu, Fengping
AU - Erro, Roberto
AU - Amboni, Marianna
AU - Pappata, Sabina
AU - Quarantelli, Mario
AU - Annesi, Grazia
AU - Quattrone, Aldo
AU - Chien, Hsin F.
AU - Barbosa, Egberto R.
AU - Oostra, Ben A.
AU - Barone, Paolo
AU - Wang, Jun
AU - Bonifati, Vincenzo
PY - 2013
Y1 - 2013
KW - Parkinsonism
KW - dystonia
KW - dementia
KW - SYNJ1
KW - PINK1
KW - gene
KW - mutation
U2 - 10.1002/humu.22373
DO - 10.1002/humu.22373
M3 - Journal article
C2 - 23804577
VL - 34
SP - 1208
EP - 1215
JO - Human Mutation
JF - Human Mutation
SN - 1059-7794
IS - 9
ER -
