ClC-1 mutations in myotonia congenita patients: insights into molecular gating mechanisms and genotype-phenotype correlation.
about
Human Aquaporin-4 and Molecular Modeling: Historical Perspective and View to the FutureTherapeutic Approaches to Genetic Ion Channelopathies and Perspectives in Drug DiscoveryMultidisciplinary study of a new ClC-1 mutation causing myotonia congenita: a paradigm to understand and treat ion channelopathiesProteomic profiling of muscle fibre type shifting in neuromuscular diseases.Understanding complexity of physiology by combined molecular simulations and experiments: anion channels as a proof of concept.Mapping ligand binding pockets in chloride ClC-1 channels through an integrated in silico and experimental approach using anthracene-9-carboxylic acid and niflumic acid.Genotype-phenotype correlation of F484L mutation in three Italian families with Thomsen myotonia.
P2860
Q26740107-B905C6C7-8CE3-47CD-A8F8-5796112EA7FFQ26744730-6C2FCC15-49EB-4D4F-A9FF-8B08DD8BA8B9Q41101211-51194A32-66C6-4116-868D-0011195A4517Q51664676-EB387A03-ED1A-4746-B826-E705CFDE1383Q51727452-2E524095-3F56-4B11-84BF-63E88453CA15Q52676150-39CF04DC-93E5-4607-BF29-589B56A3FCB1Q54105827-B0936169-7886-47DB-A05F-832659DEA70A
P2860
ClC-1 mutations in myotonia congenita patients: insights into molecular gating mechanisms and genotype-phenotype correlation.
description
2015 nî lūn-bûn
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2015年論文
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name
ClC-1 mutations in myotonia co ...... enotype-phenotype correlation.
@en
type
label
ClC-1 mutations in myotonia co ...... enotype-phenotype correlation.
@en
prefLabel
ClC-1 mutations in myotonia co ...... enotype-phenotype correlation.
@en
P2093
P2860
P50
P356
P1476
ClC-1 mutations in myotonia co ...... genotype-phenotype correlation
@en
P2093
C Altamura
D Conte Camerino
G Annicchiarico
G Lauria Pinter
M M Dinardo
R Brugnoni
P2860
P304
P356
10.1113/JP270358
P407
P50
P577
2015-07-14T00:00:00Z