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  2. www.liebertpub.com www.liebertpub.com
    Clinical and Molecular Characterization of Infantile-Onset Pompe Disease in Mainland Chinese Patients: Identification of Two Common Mutations | Genetic Testing and Molecular Biomarkers
    1
    1. ClingenBaseline 21 Oct 2026
      PD03

      Patient3: Male, northern China

      CasePresentingHPOs:

      HPOsFreeText: IOPD

      CaseNotHPOs:

      NotHPOsFreeText:

      CaseAddInfo:

      CasePMIDs:

      CasePreviousTesting: same as group

      CaseGenotypingMethod: same as group

      Variant1: NM_000152.3:c.2024A>G

      CAID: CA401370120, http://reg.clinicalgenome.org/redmine/projects/registry/genboree_registry/by_caid?caid=CA401370120

      gnomAD: n/a

      Variant2: NM_000152.4(GAA):c.2132C>G (p.Thr711Arg)

      ClinVar: 381006, https://www.ncbi.nlm.nih.gov/clinvar/variation/381006/

      gnomAD: 0.0001488, http://exac.broadinstitute.org/variant/17-78087108-C-G

      Individual CaseInfo Variant CA401370120 ClinVarID:382006 inferred_gene_hgnc:4065 inferred_gene_source:CAID GAA variant
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    liebertpub.com/doi/full/10.1089/gtmb.2016.0424
  3. www.liebertpub.com www.liebertpub.com
    Clinical and Molecular Characterization of Infantile-Onset Pompe Disease in Mainland Chinese Patients: Identification of Two Common Mutations | Genetic Testing and Molecular Biomarkers
    1
    1. ClingenBaseline 21 Oct 2026
      PD03

      Patient3: Male, northern China

      CasePresentingHPOs:

      HPOsFreeText: IOPD

      CaseNotHPOs:

      NotHPOsFreeText:

      CaseAddInfo:

      CasePMIDs:

      CasePreviousTesting: same as group

      CaseGenotypingMethod: same as group

      Variant1: NM_000152.3:c.2024A>G

      CAID: CA401370120, http://reg.clinicalgenome.org/redmine/projects/registry/genboree_registry/by_caid?caid=CA401370120

      gnomAD: n/a

      Variant2: NM_000152.4(GAA):c.2132C>G (p.Thr711Arg)

      ClinVar: 381006, https://www.ncbi.nlm.nih.gov/clinvar/variation/381006/

      gnomAD: 0.0001488, http://exac.broadinstitute.org/variant/17-78087108-C-G

      Individual CaseInfo Variant CA401370120 ClinVarID:381006 inferred_gene_hgnc:4065 inferred_gene_source:CAID GAA variant
    Visit annotations in context

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    URL

    liebertpub.com/doi/full/10.1089/gtmb.2016.0424