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A recurrent de novo ATP5F1A substitution associated with ne..:
Lines, Matthew A.
;
Cuillerier, Alexanne
;
Chakraborty, Pranesh
...
European Journal of Human Genetics. 29 (2021) 11 - p. 1719-1724 , 2021
Link:
https://doi.org/10.1038/s41431-021-00956-0
RT Journal T1
A recurrent de novo ATP5F1A substitution associated with neonatal complex V deficiency
UL https://suche.suub.uni-bremen.de/peid=cr-10.1038_s41431-021-00956-0&Exemplar=1&LAN=DE A1 Lines, Matthew A. A1 Cuillerier, Alexanne A1 Chakraborty, Pranesh A1 Naas, Turaya A1 Duque Lasio, M. Laura A1 Michaud, Jean A1 Pileggi, Chantal A1 Harper, Mary-Ellen A1 Burelle, Yan A1 Toler, Tomi L. A1 Sondheimer, Neal A1 Crawford, Heather P. A1 Millan, Francisca A1 Geraghty, Michael T. PB Springer Science and Business Media LLC YR 2021 SN 1018-4813 SN 1476-5438 JF European Journal of Human Genetics VO 29 IS 11 SP 1719 OP 1724 LK http://dx.doi.org/https://doi.org/10.1038/s41431-021-00956-0 DO https://doi.org/10.1038/s41431-021-00956-0 SF ELIB - SuUB Bremen
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