N. Keller Et Al. , "De novo DNM1L variant presenting with severe muscular atrophy, dystonia and sensory neuropathy," EUROPEAN JOURNAL OF MEDICAL GENETICS , vol.64, no.2, 2021
Keller, N. Et Al. 2021. De novo DNM1L variant presenting with severe muscular atrophy, dystonia and sensory neuropathy. EUROPEAN JOURNAL OF MEDICAL GENETICS , vol.64, no.2 .
Keller, N., Paketci, C., Edem, P., Thiele, H., YİŞ, U., Wirth, B., ... Karakaya, M.(2021). De novo DNM1L variant presenting with severe muscular atrophy, dystonia and sensory neuropathy. EUROPEAN JOURNAL OF MEDICAL GENETICS , vol.64, no.2.
Keller, Natalie Et Al. "De novo DNM1L variant presenting with severe muscular atrophy, dystonia and sensory neuropathy," EUROPEAN JOURNAL OF MEDICAL GENETICS , vol.64, no.2, 2021
Keller, Natalie Et Al. "De novo DNM1L variant presenting with severe muscular atrophy, dystonia and sensory neuropathy." EUROPEAN JOURNAL OF MEDICAL GENETICS , vol.64, no.2, 2021
Keller, N. Et Al. (2021) . "De novo DNM1L variant presenting with severe muscular atrophy, dystonia and sensory neuropathy." EUROPEAN JOURNAL OF MEDICAL GENETICS , vol.64, no.2.
@article{article, author={Natalie Keller Et Al. }, title={De novo DNM1L variant presenting with severe muscular atrophy, dystonia and sensory neuropathy}, journal={EUROPEAN JOURNAL OF MEDICAL GENETICS}, year=2021}