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STRUCTURAL AND CONTROL GENE DEFECTS IN HEREDITARY DISEASES IN MAN

โœ Scribed by Epstein, CharlesJ.


Book ID
122821039
Publisher
The Lancet
Year
1964
Tongue
English
Weight
368 KB
Volume
284
Category
Article
ISSN
0140-6736

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## Communicated by Peter Byers Hereditary coproporphyria (HC) is an acute hepatic porphyria with autosomal dominant inheritance caused by deficient activity of coproporphyrinogen III oxidase (CPO). Clinical manifestations of the disease are characterized by acute attacks of neurological dysfunctio