Journal article
Authors list: Lal, Dennis; Becker, Kerstin; Motameny, Susanne; Altmueller, Janine; Thiele, Holger; Nuernberg, Peter; Ahting, Uwe; Rolinski, Boris; Neubauer, Bernd A.; Hahn, Andreas
Publication year: 2013
Pages: 85-87
Journal: neurogenetics
Volume number: 14
Issue number: 1
ISSN: 1364-6745
DOI Link: https://doi.org/10.1007/s10048-013-0355-z
Publisher: Springer
Citation Styles
Harvard Citation style: Lal, D., Becker, K., Motameny, S., Altmueller, J., Thiele, H., Nuernberg, P., et al. (2013) Homozygous missense mutation of NDUFV1 as the cause of infantile bilateral striatal necrosis, neurogenetics, 14(1), pp. 85-87. https://doi.org/10.1007/s10048-013-0355-z
APA Citation style: Lal, D., Becker, K., Motameny, S., Altmueller, J., Thiele, H., Nuernberg, P., Ahting, U., Rolinski, B., Neubauer, B., & Hahn, A. (2013). Homozygous missense mutation of NDUFV1 as the cause of infantile bilateral striatal necrosis. neurogenetics. 14(1), 85-87. https://doi.org/10.1007/s10048-013-0355-z
Keywords
COMPLEX-I DEFICIENCY