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PP03.2 – 2683: Next generation sequencing allows the identi..:
Escobar, J.D. Ortigoza
;
Oyarzabal, A.
;
Montero, R.
...
European Journal of Paediatric Neurology. 19 (2015) - p. S36-S37 , 2015
Link:
https://doi.org/10.1016/s1090-3798(15)30118-5
RT Journal T1
PP03.2 – 2683: Next generation sequencing allows the identification of NDUFS4 defect in a patient with fatal early Leigh syndrome and deficiencies in pyruvate dehydrogenase and multiple respiratory chain complexes
UL https://suche.suub.uni-bremen.de/peid=cr-10.1016_s1090-3798(15)30118-5&Exemplar=1&LAN=DE A1 Escobar, J.D. Ortigoza A1 Oyarzabal, A. A1 Montero, R. A1 Artuch, R. A1 Gort, L. A1 Briones, P. A1 González, B. Pérez A1 Rodriguez-Pombo, P. A1 Dueñas, B. Pérez PB Elsevier BV YR 2015 SN 1090-3798 JF European Journal of Paediatric Neurology VO 19 SP S36 OP S37 LK http://dx.doi.org/https://doi.org/10.1016/s1090-3798(15)30118-5 DO https://doi.org/10.1016/s1090-3798(15)30118-5 SF ELIB - SuUB Bremen
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