TY  - GEN
AU  - Procaccio,V
AU  - Mousson,B
AU  - Beugnot,R
AU  - Duborjal,H
AU  - Feillet,F
AU  - Putet,G
AU  - Pignot-Paintrand,I
AU  - Lombès,A
AU  - De Coo,R
AU  - Smeets,H
AU  - Lunardi,J
AU  - Issartel,J P
TI  - Nuclear DNA origin of mitochondrial complex I deficiency in fatal infantile lactic acidosis evidenced by transnuclear complementation of cultured fibroblasts
SN  - 0021-9738
PY  - 1999///0805
KW  - Acidosis, Lactic
KW  - congenital
KW  - Cell Nucleus
KW  - chemistry
KW  - Cells, Cultured
KW  - DNA
KW  - genetics
KW  - DNA Mutational Analysis
KW  - DNA, Complementary
KW  - DNA, Mitochondrial
KW  - Electron Transport
KW  - Fatal Outcome
KW  - Fibroblasts
KW  - enzymology
KW  - Genetic Complementation Test
KW  - Genetic Heterogeneity
KW  - Humans
KW  - Hybrid Cells
KW  - Infant
KW  - Infant, Newborn
KW  - Male
KW  - Microscopy, Electron
KW  - NAD(P)H Dehydrogenase (Quinone)
KW  - deficiency
KW  - Organ Specificity
KW  - Transcription, Genetic
N1  - Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1172/JCI6184
ER  -