Labalme, A. Et Al. 2020. Novel progressive myoclonus epilepsy syndrome caused by a recurrent homozygous variant of SLC7A6OS. EUROPEAN JOURNAL OF HUMAN GENETICS , vol.28, no.SUPPL 1 , 414.

Labalme, A., Mazzola, L., Muona, M., BAYKAL, B., Joensuu, T. H., Courage, C., ... Chatron, N.(2020). Novel progressive myoclonus epilepsy syndrome caused by a recurrent homozygous variant of SLC7A6OS. EUROPEAN JOURNAL OF HUMAN GENETICS , vol.28, no.SUPPL 1, 414.

Labalme, A. Et Al. "Novel progressive myoclonus epilepsy syndrome caused by a recurrent homozygous variant of SLC7A6OS," EUROPEAN JOURNAL OF HUMAN GENETICS , vol.28, no.SUPPL 1, 414, 2020

Labalme, A. Et Al. "Novel progressive myoclonus epilepsy syndrome caused by a recurrent homozygous variant of SLC7A6OS." EUROPEAN JOURNAL OF HUMAN GENETICS , vol.28, no.SUPPL 1, pp.414, 2020

Labalme, A. Et Al. (2020) . "Novel progressive myoclonus epilepsy syndrome caused by a recurrent homozygous variant of SLC7A6OS." EUROPEAN JOURNAL OF HUMAN GENETICS , vol.28, no.SUPPL 1, p.414.

@article{article, author={A. Labalme Et Al. }, title={Novel progressive myoclonus epilepsy syndrome caused by a recurrent homozygous variant of SLC7A6OS}, journal={EUROPEAN JOURNAL OF HUMAN GENETICS}, year=2020, pages={414} }