Difference between revisions of "Meldau S"
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{{Person}} | {{Person | ||
|lastname=Meldau | |||
|firstname=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 | |||
|area code=7925 | |||
|city=Cape Town | |||
|country=South Africa | |||
|mailaddress=surita.meldau@uct.ac.za | |||
}} | |||
{{Labelingperson}} | |||
==Participated at == | |||
::::* [[IOC99 | IOC99 Cape Town ZA]] | |||
::::* [[MiPschool Cape Town 2015 | MiPschool 2015 Cape Town ZA]] |
Latest revision as of 11:39, 14 February 2018
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 | |
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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 | |
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Meldau 2015 Abstract MiPschool Cape Town 2015 | 2015 | Mitochondrial molecular diagnostics in South Africa: Lessons from the past 20 years. |