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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‎Updated Item: Adding statements: cites work (P2860)
Property / cites work
 
Property / cites work: The phenotype of calpainopathy: diagnosis based on a multidisciplinary approach / rank
 
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Property / cites work: The phenotype of calpainopathy: diagnosis based on a multidisciplinary approach / reference
 
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Property / cites work: Novel mutations in the calpain 3 gene in Germany / rank
 
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Property / cites work: Novel mutations in the calpain 3 gene in Germany / reference
 
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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
 
stated in: Crossref
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Property / cites work: Analysis of histopathologic and molecular pathologic findings in Czech LGMD2A patients / rank
 
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reference URL: https://api.crossref.org/works/10.1038%2FEJHG.2008.47
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reference URL: https://api.crossref.org/works/10.1038%2FEJHG.2008.47
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Revision as of 21:10, 7 July 2021

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=1455780745"