Minnerop, M. Et Al. 2017. Hypomorphic mutations in POLR3A are a frequent cause of sporadic and recessive spastic ataxia. BRAIN , vol.140 , 1561-1578.

Minnerop, M., Kurzwelly, D., Wagner, H., Soehn, A. S., Reichbauer, J., Tao, F., ... Rattay, T. W.(2017). Hypomorphic mutations in POLR3A are a frequent cause of sporadic and recessive spastic ataxia. BRAIN , vol.140, 1561-1578.

Minnerop, Martina Et Al. "Hypomorphic mutations in POLR3A are a frequent cause of sporadic and recessive spastic ataxia," BRAIN , vol.140, 1561-1578, 2017

Minnerop, Martina Et Al. "Hypomorphic mutations in POLR3A are a frequent cause of sporadic and recessive spastic ataxia." BRAIN , vol.140, pp.1561-1578, 2017

Minnerop, M. Et Al. (2017) . "Hypomorphic mutations in POLR3A are a frequent cause of sporadic and recessive spastic ataxia." BRAIN , vol.140, pp.1561-1578.

@article{article, author={Martina Minnerop Et Al. }, title={Hypomorphic mutations in POLR3A are a frequent cause of sporadic and recessive spastic ataxia}, journal={BRAIN}, year=2017, pages={1561-1578} }