11 – 15 of 20
- show: 5
- |
- sort: year (new to old)
Close
Embed this list
<iframe src=" "
width=" "
height=" "
allowtransparency="true"
frameborder="0">
</iframe>
- 2011
-
Mark
Complex III staining in blue native polyacrylamide gels
(
- Contribution to journal › Article
-
Mark
Mitochondrial hepatopathies in the newborn period.
(
- Contribution to journal › Article
-
Mark
The GRACILE mutation introduced into Bcs1l causes postnatal complex III deficiency: A viable mouse model for mitochondrial hepatopathy.
(
- Contribution to journal › Article
- 2010
-
Mark
Bcs1L A232G mutant mice: A new model of complex III deficiency and hepatic cirrhosis
(
- Contribution to journal › Published meeting abstract
-
Mark
Characterization of complex III deficiency and liver dysfunction in GRACILE syndrome caused by a BCS1L mutation.
(
- Contribution to journal › Article