![](/img/cover-not-exists.png)
Acute intermittent porphyria caused by a G to C mutation in exon 12 of the porphobilinogen deaminase gene that results in exon skipping
Makoto Daimon, Keiichi Yamatani, Masahiko Igarashi, Norio Fukase, Atsushi Ogawa, Makoto Tominaga, Hideo SasakiVolume:
92
Language:
english
Pages:
5
DOI:
10.1007/bf00420937
Date:
December, 1993
File:
PDF, 876 KB
english, 1993