Cargando…
OR11-001 - Protein misfolding in mevalonate kinase deficiency
Autores principales: | Stojanov, S, Gersting, SW, Reitzle, L, Reiß, D, Belohradsky, BH, Vogeser, M, Maier, B, Teupser, D, Muntau, AC |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3952567/ http://dx.doi.org/10.1186/1546-0096-11-S1-A190 |
Ejemplares similares
-
PW03-021 - HSCT in mevalonate kinase deficiency
por: Wolska-Kuśnierz, B, et al.
Publicado: (2013) -
Glutaryl-CoA Dehydrogenase Misfolding in Glutaric Acidemia Type 1
por: Barroso, Madalena, et al.
Publicado: (2023) -
PW02-020 - Colitis revealing mevalonate kinase deficiency
por: Michael, L, et al.
Publicado: (2013) -
Protein misfolding is the molecular mechanism underlying MCADD identified in newborn screening
por: Maier, Esther M., et al.
Publicado: (2009) -
P03-007 - Mevalonate kinase gene in Behçet’s disease
por: Tas, D Arslan, et al.
Publicado: (2013)