Hypertrophic cardiomyopathy in young Maine Coon cats caused by the p.A31P cMyBP-C mutation--the clinical significance of having the mutation.
about
The A31P missense mutation in cardiac myosin binding protein C alters protein structure but does not cause haploinsufficiency.The genetic basis of hypertrophic cardiomyopathy in cats and humans.A One Health Approach to Hypertrophic Cardiomyopathy.Looking into a whale's heart: investigating a genetic basis for cardiomyopathy in a non-model species.Prevalence and demographics of the MYBPC3-mutations in ragdolls and Maine coons in the British Isles.Impaired cardiac mitochondrial oxidative phosphorylation and enhanced mitochondrial oxidative stress in feline hypertrophic cardiomyopathy.International collaborative study to assess cardiovascular risk and evaluate long-term health in cats with preclinical hypertrophic cardiomyopathy and apparently healthy cats: The REVEAL Study.
P2860
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P2860
Hypertrophic cardiomyopathy in young Maine Coon cats caused by the p.A31P cMyBP-C mutation--the clinical significance of having the mutation.
description
2011 nî lūn-bûn
@nan
2011 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Hypertrophic cardiomyopathy in ...... icance of having the mutation.
@ast
Hypertrophic cardiomyopathy in ...... icance of having the mutation.
@en
Hypertrophic cardiomyopathy in ...... icance of having the mutation.
@nl
type
label
Hypertrophic cardiomyopathy in ...... icance of having the mutation.
@ast
Hypertrophic cardiomyopathy in ...... icance of having the mutation.
@en
Hypertrophic cardiomyopathy in ...... icance of having the mutation.
@nl
prefLabel
Hypertrophic cardiomyopathy in ...... icance of having the mutation.
@ast
Hypertrophic cardiomyopathy in ...... icance of having the mutation.
@en
Hypertrophic cardiomyopathy in ...... icance of having the mutation.
@nl
P2093
P2860
P356
P1476
Hypertrophic cardiomyopathy in ...... ficance of having the mutation
@en
P2093
Mia T N Godiksen
Michael Christiansen
Sara Granstrøm
P2860
P2888
P356
10.1186/1751-0147-53-7
P50
P577
2011-02-09T00:00:00Z
P5875
P6179
1014186520