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Journal description
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Details for article 10 of 21 found articles
| Title: |
Diverse phenotype in patients with complex I deficiency due to mutations in NDUFB11 |
| Author: |
Reinson, Karit Kovacs-Nagy, Reka Õiglane-Shlik, Eve Pajusalu, Sander Nõukas, Margit Wintjes, Liesbeth T. van den Brandt, Frans C.A. Brink, Maaike Acker, Till Ahting, Uwe Hahn, Andreas Schänzer, Anne Haack, Tobias B. Rodenburg, Richard J. Õunap, Katrin |
| Appeared in: |
European journal of medical genetics |
| Paging: | Volume 62 (2019) nr. 11 pages p. |
| Year: |
2019 |
| Contents: | |
| Publisher: |
Elsevier Masson SAS |
| Source file: |
Elektronische Wetenschappelijke Tijdschriften |
Details for article 10 of 21 found articles
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