Kuipers, D. Et Al. 2019. Late-onset phenotype associated with a homozygous GJC2 missense mutation in a Turkish family. PARKINSONISM & RELATED DISORDERS , vol.66 , 228-231.

Kuipers, D., Tufekcioglu, Z., Bilgiç, B., Olgiati, S., Dremmen, M., van, I., ... Breedveld, G.(2019). Late-onset phenotype associated with a homozygous GJC2 missense mutation in a Turkish family. PARKINSONISM & RELATED DISORDERS , vol.66, 228-231.

Kuipers, DJS Et Al. "Late-onset phenotype associated with a homozygous GJC2 missense mutation in a Turkish family," PARKINSONISM & RELATED DISORDERS , vol.66, 228-231, 2019

Kuipers, DJS Et Al. "Late-onset phenotype associated with a homozygous GJC2 missense mutation in a Turkish family." PARKINSONISM & RELATED DISORDERS , vol.66, pp.228-231, 2019

Kuipers, D. Et Al. (2019) . "Late-onset phenotype associated with a homozygous GJC2 missense mutation in a Turkish family." PARKINSONISM & RELATED DISORDERS , vol.66, pp.228-231.

@article{article, author={DJS Kuipers Et Al. }, title={Late-onset phenotype associated with a homozygous GJC2 missense mutation in a Turkish family}, journal={PARKINSONISM & RELATED DISORDERS}, year=2019, pages={228-231} }