M. Karakaya Et Al. , "Variants causing mitochondrial dysfunction are not rare in non-5q SMA: Re-evaluation of thirty families by exome sequencing," EUROPEAN JOURNAL OF HUMAN GENETICS , vol.28, pp.442, 2020
Karakaya, M. Et Al. 2020. Variants causing mitochondrial dysfunction are not rare in non-5q SMA: Re-evaluation of thirty families by exome sequencing. EUROPEAN JOURNAL OF HUMAN GENETICS , vol.28 , 442.
Karakaya, M., Keller, N., Altmueller, J., Motameny, S., Thiele, H., Wunderlich, G., ... Kirschner, J.(2020). Variants causing mitochondrial dysfunction are not rare in non-5q SMA: Re-evaluation of thirty families by exome sequencing. EUROPEAN JOURNAL OF HUMAN GENETICS , vol.28, 442.
Karakaya, M. Et Al. "Variants causing mitochondrial dysfunction are not rare in non-5q SMA: Re-evaluation of thirty families by exome sequencing," EUROPEAN JOURNAL OF HUMAN GENETICS , vol.28, 442, 2020
Karakaya, M. Et Al. "Variants causing mitochondrial dysfunction are not rare in non-5q SMA: Re-evaluation of thirty families by exome sequencing." EUROPEAN JOURNAL OF HUMAN GENETICS , vol.28, pp.442, 2020
Karakaya, M. Et Al. (2020) . "Variants causing mitochondrial dysfunction are not rare in non-5q SMA: Re-evaluation of thirty families by exome sequencing." EUROPEAN JOURNAL OF HUMAN GENETICS , vol.28, p.442.
@article{article, author={M. Karakaya Et Al. }, title={Variants causing mitochondrial dysfunction are not rare in non-5q SMA: Re-evaluation of thirty families by exome sequencing}, journal={EUROPEAN JOURNAL OF HUMAN GENETICS}, year=2020, pages={442} }