Akizu, N. Et Al. 2015. Biallelic mutations in SNX14 cause a syndromic form of cerebellar atrophy and lysosome-autophagosome dysfunction. NATURE GENETICS , vol.47, no.5 , 528-536.

Akizu, N., Cantagrel, V., Zaki, M. S., Al-Gazali, L., Wang, X., Rosti, R. O., ... Dikoglu, E.(2015). Biallelic mutations in SNX14 cause a syndromic form of cerebellar atrophy and lysosome-autophagosome dysfunction. NATURE GENETICS , vol.47, no.5, 528-536.

Akizu, Naiara Et Al. "Biallelic mutations in SNX14 cause a syndromic form of cerebellar atrophy and lysosome-autophagosome dysfunction," NATURE GENETICS , vol.47, no.5, 528-536, 2015

Akizu, Naiara Et Al. "Biallelic mutations in SNX14 cause a syndromic form of cerebellar atrophy and lysosome-autophagosome dysfunction." NATURE GENETICS , vol.47, no.5, pp.528-536, 2015

Akizu, N. Et Al. (2015) . "Biallelic mutations in SNX14 cause a syndromic form of cerebellar atrophy and lysosome-autophagosome dysfunction." NATURE GENETICS , vol.47, no.5, pp.528-536.

@article{article, author={Naiara Akizu Et Al. }, title={Biallelic mutations in SNX14 cause a syndromic form of cerebellar atrophy and lysosome-autophagosome dysfunction}, journal={NATURE GENETICS}, year=2015, pages={528-536} }