Glycogen storage disease type II: identifation of a dinucleotide deletion and a common missense mutation in the lysosomal alpha-glucosidase gene

Marian Haan, D (Dik) van Leenen, J (J.) Verbiest, Arnold Reuser, MMP (Monique) Hermans

Research output: Contribution to journalArticleAcademicpeer-review

Original languageUndefined/Unknown
Pages (from-to)379-382
Number of pages4
JournalClinical Genetics
Publication statusPublished - 1998

Research programs

  • EMC MGC-02-96-01
  • EMC MM-03-54-04-A

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