Ancestral founder of mutation W283X in the porphobilinoge deaminase gene among acute intermittent porphyria patient.

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dc.contributor.authorSchneider-Yin X
dc.contributor.authorHergersberg M
dc.contributor.authorGoldgar DE
dc.contributor.authorRufenacht UB
dc.contributor.authorSchuurmans M
dc.contributor.authorPuy H
dc.contributor.authorDeybach JC
dc.contributor.authorMinder EI
dc.date.accessioned2013-01-23T11:52:22Z
dc.date.available2013-01-23T11:52:22Z
dc.date.issued2002
dc.descriptionGesondheidswetenskappe
dc.descriptionInterne Geneeskunde
dc.descriptionPlease help us populate SUNScholar with the post print version of this article. It can be e-mailed to: scholar@sun.ac.za
dc.identifier.citationHuman Heredity
dc.identifier.urihttp://hdl.handle.net/10019.1/76412
dc.publisherKARGER, ALLSCHWILERSTRASSE 10, BASEL, SWITZERLAND, CH-4009
dc.titleAncestral founder of mutation W283X in the porphobilinoge deaminase gene among acute intermittent porphyria patient.
dc.typeJournal Articles (subsidised)
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