Identification of a Prevalent Nonsense Mutation (W283X) and Two Novel Mutations in the Porphobilinogen Deaminase Gene of Swiss Patients with Acute Intermittent Porphyria

Publisher： Karger

E-ISSN： 1423-0062|50|4|247-250

ISSN： 0001-5652

Source： Human Heredity, Vol.50, Iss.4, 2000-04, pp. : 247-250

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