cDNA analyses of CAPN3 enhance mutation detection and reveal a low prevalence of LGMD2A patients in Denmark (Q50547039): Difference between revisions

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‎Created claim: exact match (P2888): https://scigraph.springernature.com/pub.10.1038/ejhg.2008.47, batch #16484
‎Set a claim value: title (P1476): cDNA analyses of CAPN3 enhance mutation detection and reveal a low prevalence of LGMD2A patients in Denmark
 
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label / enlabel / en
cDNA analyses of CAPN3 enhance mutation detection and reveal a low prevalence of LGMD2A patients in Denmark.
cDNA analyses of CAPN3 enhance mutation detection and reveal a low prevalence of LGMD2A patients in Denmark
label / nllabel / nl
cDNA analyses of CAPN3 enhance mutation detection and reveal a low prevalence of LGMD2A patients in Denmark.
cDNA analyses of CAPN3 enhance mutation detection and reveal a low prevalence of LGMD2A patients in Denmark
description / hydescription / hy
 
2008 թվականի մարտի 12-ին հրատարակված գիտական հոդված
Property / titleProperty / title
cDNA analyses of CAPN3 enhance mutation detection and reveal a low prevalence of LGMD2A patients in Denmark. (English)
cDNA analyses of CAPN3 enhance mutation detection and reveal a low prevalence of LGMD2A patients in Denmark (English)
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John Vissing
 
Property / author name string: John Vissing / rank
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Property / author name string: John Vissing / qualifier
 
Property / author name string: John Vissing / reference
stated in: Europe PubMed Central
PubMed publication ID: 18337726
retrieved: 15 March 2018
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reference URL: http://europepmc.org/abstract/MED/18337726
 
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Property / cites work: The phenotype of calpainopathy: diagnosis based on a multidisciplinary approach / rank
 
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Property / cites work: Novel mutations in the calpain 3 gene in Germany / rank
 
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Property / cites work: Screening of the CAPN3 gene in patients with possible LGMD2A / rank
 
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Property / cites work: Screening of the CAPN3 gene in patients with possible LGMD2A / reference
 
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Property / cites work: Analysis of histopathologic and molecular pathologic findings in Czech LGMD2A patients / rank
 
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Property / cites work: Protein- and mRNA-based phenotype-genotype correlations in DMD/BMD with point mutations and molecular basis for BMD with nonsense and frameshift mutations in the DMD gene / rank
 
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Property / cites work: Protein- and mRNA-based phenotype-genotype correlations in DMD/BMD with point mutations and molecular basis for BMD with nonsense and frameshift mutations in the DMD gene / reference
 
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Property / cites work: A family with McLeod syndrome and calpainopathy with clinically overlapping diseases / rank
 
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reference URL: http://europepmc.org/abstract/MED/18337726

Latest revision as of 00:36, 25 September 2024

scientific article published on 12 March 2008
Language Label Description Also known as
English
cDNA analyses of CAPN3 enhance mutation detection and reveal a low prevalence of LGMD2A patients in Denmark
scientific article published on 12 March 2008

    Statements

    title
    cDNA analyses of CAPN3 enhance mutation detection and reveal a low prevalence of LGMD2A patients in Denmark (English)
    1 reference
    stated in
    Europe PubMed Central
    PubMed publication ID
    18337726
    retrieved
    15 March 2018
    reference URL
    http://europepmc.org/abstract/MED/18337726
    main subject
    Denmark
    0 references
    cites work

    Identifiers

     
                      Retrieved from "https://www.wikidata.org/w/index.php?title=Q50547039&oldid=2252559147"