A novel 12-base pair deletion mutation in exon 15 of the porphobilinogen deaminase gene in a Taiwanese patient with acute intermittent porphyria. Blood cells, molecules & diseases [Blood Cells Mol Dis] Journal article | | Title | A novel 12-base pair deletion mutation in exon 15 of the porphobilinogen deaminase gene in a Taiwanese patient with acute intermittent porphyria. | | Author(s) | Sakabe JI, Susa S, Daimon M, Lan MY, Kato T | | Institution | Department of Neurology, Hematology, Metabolism, Endocrinology and Diabetology (DNHMED), Yamagata University School of Medicine, 2-2-2 Iida-Nishi, Yamagata 990-9585, Japan. | | Source | Blood Cells Mol Dis 2008 Jun 11. | | Language | ENG | | Pub Type(s) | LETTER
| | PubMed ID | 18554962 |
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