- oxidoreductase,
mitochondrial is an
enzyme that in
humans is
encoded by the
ETFDH gene. This gene
encodes a
component of the electron-transfer
system in mitochondria...
-
fibres and
deficiency of
coenzyme Q10.
Mutations in the ETFA, ETFB, and
ETFDH genes cause glutaric acidemia type II.
Mutations in
these genes result in...
-
transfer flavoprotein-ubiquinone
oxidoreductase (ETF-QO)
encoded by the
ETFDH gene. ETF-QO
subsequently relays the
electrons via
ubiquinone to complex...
-
affected by
other genetic defects (such as
mutations of
mitochondrial DNA,
ETFDH, APTX, FXN, and BRAF,
genes that are not
directly related to the CoQ10 biosynthetic...
- and
contains a
flavin and FE-S cluster. In humans, it is
encoded by the
ETFDH gene.
Deficiency in ETF
dehydrogenase causes the
human genetic disease multiple...
-
transfer flavoprotein-ubiquinone
oxidoreductase (ETF-QO)
encoded by the
ETFDH gene. ETF-QO
subsequently relays the
electrons via
ubiquinone to complex...
-
Gillespie syndrome PAX6
Glutaric aciduria, type I and type 2 GCDH, ETFA, ETFB,
ETFDH recessive GRACILE syndrome BCS1L GRIN2B-related
neurodevelopmental disorder...
- Glutaricaciduria, type IIB; 231680; ETFB Glutaricaciduria, type IIC; 231680;
ETFDH Glutathione synthetase deficiency; 266130; GSS
Glycerol kinase deficiency;...
- MADD is a
genetic disorder,
caused by a
mutation in the ETFA, ETFB, and
ETFDH genes. MADD is
known as an "autosomal
recessive disorder"
because for one...
- HGNC:3481 P13804 5127 ETFB HGNC:3482 P38117 5128
ETFBKMT HGNC:28739 Q8IXQ9 5129
ETFDH HGNC:3483 Q16134 5130 ETFRF1 HGNC:27052 Q6IPR1 5131 ETHE1 HGNC:23287 O95571...
