Difference between revisions of "Meldau S"
From Bioblast
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|institution=Medical Scientist (M.Sc Med): Chemical Pathology | |institution=Medical Scientist (M.Sc Med): Chemical Pathology | ||
UCT/NHLS Inherited Metabolic Diseases Laboratory | UCT/NHLS Inherited Metabolic Diseases Laboratory | ||
|address=Room 6.39 Falmouth Building | |address=Room 6.39 Falmouth Building | ||
University of Cape Town Medical School | University of Cape Town Medical School | ||
Observatory | Observatory | ||
|area code=7925 | |area code=7925 | ||
|city=Cape Town | |city=Cape Town | ||
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* [[IOC99 | IOC99 Cape Town ZA]] | * [[IOC99 | IOC99 Cape Town ZA]] | ||
* [[MiPschool Cape Town 2015 | MiPschool 2015 Cape Town ZA]] | |||
Revision as of 15:15, 31 May 2016
| Name | Meldau Surita, |
|---|---|
| Institution | Medical Scientist (M.Sc Med): Chemical Pathology
UCT/NHLS Inherited Metabolic Diseases Laboratory |
| Address | Room 6.39 Falmouth Building
University of Cape Town Medical School Observatory, 7925 |
| City | Cape Town |
| State/Province | |
| Country | South Africa |
| surita.meldau@uct.ac.za | |
| Weblink | |
| O2k-Network Lab |
Labels:
Publications
| Published | Reference | |
|---|---|---|
| Meldau 2024 Mol Genet Metab Rep | 2024 | Meldau S, Ackermann S, Riordan G, van der Watt GF, Spencer C, Raga S, Khan K, Blackhurst DM, van der Westhuizen FH (2024) A novel mitochondrial DNA variant in MT-ND6: m.14430A>C p.(Trp82Gly) identified in a patient with Leigh syndrome and complex I deficiency. Mol Genet Metab Rep 39:101078. https://doi.org/10.1016/j.ymgmr.2024.101078 |
Abstracts
| Published | Reference | |
|---|---|---|
| Meldau 2015 Abstract MiPschool Cape Town 2015 | 2015 | Mitochondrial molecular diagnostics in South Africa: Lessons from the past 20 years. |
