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Two novel mutations and coexistence of the 991C.T and the 1339C.T mutation on a single allele in the coproporphyrinogen oxidase gene in Swedish patients with hereditary coproporphyria

✍ Scribed by Å. Wiman; Y. Floderus; P. Harper

Publisher: Nature Publishing Group
Year: 2002
Tongue: English
Weight: 73 KB
Volume: 47
Category: Article
ISSN: 1435-232X
DOI: 10.1007/s100380200059

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