TY  - JOUR 
AU  - Bravo-Alonso, I.
AU  - Navarrete, R.
AU  - Vega, A. I.
AU  - Ruíz-Sala, P.
AU  - García Silva, M. T.
AU  - Martín-Hernández, E.
AU  - Quijada-Fraile, P.
AU  - Belanger-Quintana, A.
AU  - Stanescu, S.
AU  - Bueno, M.
AU  - Vitoria, I.
AU  - Toledo, L.
AU  - Couce Pico,  María Luz
AU  - García-Jiménez, I.
AU  - Ramos-Ruiz, R.
AU  - Martín, M.
AU  - Desviat, L. R.
AU  - Ugarte, M.
AU  - Pérez-Cerdá, C.
AU  - Merinero, B.
AU  - Pérez, B.
AU  - Rodríguez-Pombo, P.
PY  - 2019
SN  - 2077-0383
UR  - http://hdl.handle.net/20.500.11940/15381
AB  - Congenital lactic acidosis (CLA) is a rare condition in most instances due to a range of inborn errors of metabolism that result in defective mitochondrial function. Even though the implementation of next generation sequencing has been rapid, the...
LA  - eng
TI  - Genes and Variants Underlying Human Congenital Lactic Acidosis-From Genetics to Personalized Treatment
DO  - 10.3390/jcm8111811
T2  - Journal of Clinical Medicine
M2  - 1811
KW  - CHUS
KW  - IDIS
VL  - 8
ER  -