F. Akcimen Et Al. , "A novel homozygous FBXO38 variant causes an early-onset distal hereditary motor neuronopathy type IID.," Journal of human genetics , vol.64, no.11, pp.1141-1144, 2019
Akcimen, F. Et Al. 2019. A novel homozygous FBXO38 variant causes an early-onset distal hereditary motor neuronopathy type IID.. Journal of human genetics , vol.64, no.11 , 1141-1144.
Akcimen, F., Vural, A., Durmus, H., Cakar, A., Houlden, H., Parman, Y. G., ... Basak, A. N.(2019). A novel homozygous FBXO38 variant causes an early-onset distal hereditary motor neuronopathy type IID.. Journal of human genetics , vol.64, no.11, 1141-1144.
Akcimen, Fulya Et Al. "A novel homozygous FBXO38 variant causes an early-onset distal hereditary motor neuronopathy type IID.," Journal of human genetics , vol.64, no.11, 1141-1144, 2019
Akcimen, Fulya Et Al. "A novel homozygous FBXO38 variant causes an early-onset distal hereditary motor neuronopathy type IID.." Journal of human genetics , vol.64, no.11, pp.1141-1144, 2019
Akcimen, F. Et Al. (2019) . "A novel homozygous FBXO38 variant causes an early-onset distal hereditary motor neuronopathy type IID.." Journal of human genetics , vol.64, no.11, pp.1141-1144.
@article{article, author={Fulya Akcimen Et Al. }, title={A novel homozygous FBXO38 variant causes an early-onset distal hereditary motor neuronopathy type IID.}, journal={Journal of human genetics}, year=2019, pages={1141-1144} }