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Clinical, biochemical, cellular and molecular characterizat..:
Uusimaa, Johanna
;
Evans, Julie
;
Smith, Conrad
...
European Journal of Human Genetics. 22 (2013) 2 - p. 184-191 , 2013
Link:
https://doi.org/10.1038/ejhg.2013.112
RT Journal T1
Clinical, biochemical, cellular and molecular characterization of mitochondrial DNA depletion syndrome due to novel mutations in the MPV17 gene
UL https://suche.suub.uni-bremen.de/peid=cr-10.1038_ejhg.2013.112&Exemplar=1&LAN=DE A1 Uusimaa, Johanna A1 Evans, Julie A1 Smith, Conrad A1 Butterworth, Anna A1 Craig, Kate A1 Ashley, Neil A1 Liao, Chunyan A1 Carver, Janet A1 Diot, Alan A1 Macleod, Lorna A1 Hargreaves, Iain A1 Al-Hussaini, Abdulrahman A1 Faqeih, Eissa A1 Asery, Ali A1 Al Balwi, Mohammed A1 Eyaid, Wafaa A1 Al-Sunaid, Areej A1 Kelly, Deirdre A1 van Mourik, Indra A1 Ball, Sarah A1 Jarvis, Joanna A1 Mulay, Arundhati A1 Hadzic, Nedim A1 Samyn, Marianne A1 Baker, Alastair A1 Rahman, Shamima A1 Stewart, Helen A1 Morris, Andrew AM A1 Seller, Anneke A1 Fratter, Carl PB Springer Science and Business Media LLC YR 2013 SN 1018-4813 SN 1476-5438 JF European Journal of Human Genetics VO 22 IS 2 SP 184 OP 191 LK http://dx.doi.org/https://doi.org/10.1038/ejhg.2013.112 DO https://doi.org/10.1038/ejhg.2013.112 SF ELIB - SuUB Bremen
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