Publisher
Springer Berlin Heidelberg
Reference22 articles.
1. Albers JW, Fink JK (2004) Porphyric neuropathy. Muscle Nerve 30:410–422
2. Bosma PJ (2003) Inherited disorders of bilirubin metabolism. J Hepatol 38:107–117
3. Brasch, L, Zang C, Haverkamp T, Schlechte H, Heckers H, Petrides PE (2004) Molecular analysis of acute intermittent porphyria: mutation screening in 20 patients in Germany reveals 11 novel mutations. Blood Cells, Mol Dis 32:309–314
4. Burden A, Sellers VM, Wang BC, Wu CK, Dailey HA, Rose JP, (2001) The 2.0 Å structure of human ferrochelatase, the terminal enzyme of heme biosynthesis. Nature Structural Biology 8:154–160
5. Costa E (2006) Hematologically important mutations: Bilirubin UDP-glucuronyltransferase gene mutations in Gilbert and Crigler-Najjar syndromes. Bloods Cells, Mol Dis 36: 77–80