Lohmann, E. Et Al. 2012. A homozygous frameshift mutation of sepiapterin reductase gene causing parkinsonism with onset in childhood. PARKINSONISM & RELATED DISORDERS , vol.18, no.2 , 191-193.

Lohmann, E., Koroglu, C., Hanagasi, H. A., Dursun, B., Tasan, E., & TOLUN, A., (2012). A homozygous frameshift mutation of sepiapterin reductase gene causing parkinsonism with onset in childhood. PARKINSONISM & RELATED DISORDERS , vol.18, no.2, 191-193.

Lohmann, Ebba Et Al. "A homozygous frameshift mutation of sepiapterin reductase gene causing parkinsonism with onset in childhood," PARKINSONISM & RELATED DISORDERS , vol.18, no.2, 191-193, 2012

Lohmann, Ebba Et Al. "A homozygous frameshift mutation of sepiapterin reductase gene causing parkinsonism with onset in childhood." PARKINSONISM & RELATED DISORDERS , vol.18, no.2, pp.191-193, 2012

Lohmann, E. Et Al. (2012) . "A homozygous frameshift mutation of sepiapterin reductase gene causing parkinsonism with onset in childhood." PARKINSONISM & RELATED DISORDERS , vol.18, no.2, pp.191-193.

@article{article, author={Ebba Lohmann Et Al. }, title={A homozygous frameshift mutation of sepiapterin reductase gene causing parkinsonism with onset in childhood}, journal={PARKINSONISM & RELATED DISORDERS}, year=2012, pages={191-193} }