Diverse phenotype in patients with complex I deficiency due to mutations in NDUFB11

DSpace Repository

Diverse phenotype in patients with complex I deficiency due to mutations in NDUFB11

Author: Reinson, Karit; Kovacs-Nagy, Reka; Oiglane-Shlik, Eve; Pajusalu, Sander; Noukas, Margit; Wintjes, Liesbeth T.; van den Brandt, Frans C. A.; Brink, Maaike; Acker, Till; Ahting, Uwe; Hahn, Andreas; Schanzer, Anne; Haack, Tobias B.; Rodenburg, Richard J.; Ounapa, Katrin
Tübinger Autor(en):
Haack, Tobias
Published in: European Journal of Medical Genetics (2019), Bd. 62, Article UNSP 103572
Verlagsangabe: Elsevier
Language: English
Full text: http://dx.doi.org/10.1016/j.ejmg.2018.11.006
ISSN: 1878-0849
DDC Classifikation: 570 - Life sciences; biology
610 - Medicine and health
Dokumentart: Artikel
Show full item record

This item appears in the following Collection(s)