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In frame deletion of glycin 390 in coproporphyrinogen oxidase gene as a cause of hereditary coproporphyria

✍ Scribed by R. Rosipal; E. Malonova; J. Zeman; J. Deybach; J. Lamoril; P. Martasek

Book ID: 118564542
Publisher: Elsevier Science
Year: 2001
Tongue: English
Weight: 274 KB
Volume: 34
Category: Article
ISSN: 0168-8278
DOI: 10.1016/s0168-8278(01)81707-4

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