Evidence for an ancestral founder of the common R116W mutation in the hydroxymethylbilane synthase gene in acute intermittent porphyria in The Netherlands

Research output: Contribution to journalArticleAcademicpeer-review

3 Citations (Scopus)
Original languageUndefined/Unknown
Pages (from-to)64-69
Number of pages6
JournalCellular & Molecular Biology
Volume55
DOIs
Publication statusPublished - 2009

Cite this