Glycogen storage disease type II: frequency of three common mutant alleles and their associated clinical phenotypes studied in 121 patients
- PMID: 8558570
- PMCID: PMC1051720
- DOI: 10.1136/jmg.32.10.836-a
Glycogen storage disease type II: frequency of three common mutant alleles and their associated clinical phenotypes studied in 121 patients
Comment in
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Frequency of mutations for glycogen storage disease type II in different populations: the delta525T and deltaexon 18 mutations are not generally "common" in white populations.J Med Genet. 1999 Jan;36(1):85-6. J Med Genet. 1999. PMID: 9950376 Free PMC article. No abstract available.
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