about
Identification of an Allosteric Binding Site on Human Lysosomal Alpha-Galactosidase Opens the Way to New Pharmacological Chaperones for Fabry DiseaseThe Large Phenotypic Spectrum of Fabry Disease Requires Graduated Diagnosis and Personalized Therapy: A Meta-Analysis Can Help to Differentiate Missense MutationsComputational Investigation of the Missense Mutations in DHCR7 Gene Associated with Smith-Lemli-Opitz Syndrome.Human Mitochondrial HMG-CoA Synthase Deficiency: Role of Enzyme Dimerization Surface and Characterization of Three New Patients.
P2860
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
2015年论文
@zh
2015年论文
@zh-cn
name
Taming molecular flexibility to tackle rare diseases.
@en
type
label
Taming molecular flexibility to tackle rare diseases.
@en
prefLabel
Taming molecular flexibility to tackle rare diseases.
@en
P2860
P1433
P1476
Taming molecular flexibility to tackle rare diseases
@en
P2093
Marc Baaden
P2860
P356
10.1016/J.BIOCHI.2015.03.018
P577
2015-04-02T00:00:00Z