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Overrepresentation of the founder PPOX gene mutation R59W in a South African patient with severe clinical manifestation of porphyria

✍ Scribed by J. Nico P. De Villiers; Maritha J. Kotze; Carel J. Van Heerden; Annalene Sadie; Helena F. J. Gardner; Juanita Liebenberg; René Van Zyl; Lana Du Plessis; Matti Kimberg; Jorge Frank; Louise Warnich

Book ID: 110755117
Publisher: John Wiley and Sons
Year: 2005
Tongue: English
Weight: 749 KB
Volume: 14
Category: Article
ISSN: 0906-6705
DOI: 10.1111/j.0906-6705.2005.00228.x

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