Late-onset phenotype associated with a homozygous GJC2 missense mutation in a Turkish family

Demy Kuipers; Z Tufekcioglu; B Bilgic; Simone Olgiati; Marjolein Dremmen; Wilfred van Ijcken; Guido Breedveld; Grazia Verheijen - Mancini; HA Hanagasi; M Emre; Vincenzo Bonifati

doi:10.1016/j.parkreldis.2019.07.033

Late-onset phenotype associated with a homozygous GJC2 missense mutation in a Turkish family

Demy Kuipers, Z Tufekcioglu, B Bilgic, Simone Olgiati, Marjolein Dremmen, Wilfred van Ijcken, Guido Breedveld, Grazia Verheijen - Mancini, HA Hanagasi, M Emre, Vincenzo Bonifati

Research output: Contribution to journal › Article › Academic › peer-review

4 Citations (Scopus)

Original language	Undefined/Unknown
Pages (from-to)	228-231
Number of pages	4
Journal	Parkinsonism & Related Disorders
Volume	66
DOIs	https://doi.org/10.1016/j.parkreldis.2019.07.033
Publication status	Published - 2019

Access to Document

10.1016/j.parkreldis.2019.07.033

http://hdl.handle.net/1765/119017

Cite this

@article{ac95d17844124d1788a2a6930d22142d,

title = "Late-onset phenotype associated with a homozygous GJC2 missense mutation in a Turkish family",

author = "Demy Kuipers and Z Tufekcioglu and B Bilgic and Simone Olgiati and Marjolein Dremmen and {van Ijcken}, Wilfred and Guido Breedveld and {Verheijen - Mancini}, Grazia and HA Hanagasi and M Emre and Vincenzo Bonifati",

year = "2019",

doi = "10.1016/j.parkreldis.2019.07.033",

language = "Undefined/Unknown",

volume = "66",

pages = "228--231",

journal = "Parkinsonism & Related Disorders",

issn = "1353-8020",

publisher = "Elsevier",

}

TY - JOUR

T1 - Late-onset phenotype associated with a homozygous GJC2 missense mutation in a Turkish family

AU - Kuipers, Demy

AU - Tufekcioglu, Z

AU - Bilgic, B

AU - Olgiati, Simone

AU - Dremmen, Marjolein

AU - van Ijcken, Wilfred

AU - Breedveld, Guido

AU - Verheijen - Mancini, Grazia

AU - Hanagasi, HA

AU - Emre, M

AU - Bonifati, Vincenzo

PY - 2019

Y1 - 2019

U2 - 10.1016/j.parkreldis.2019.07.033

DO - 10.1016/j.parkreldis.2019.07.033

M3 - Article

SN - 1353-8020

VL - 66

SP - 228

EP - 231

JO - Parkinsonism & Related Disorders

JF - Parkinsonism & Related Disorders

ER -