✦ LIBER ✦

Identification of Defect in the Genes for Bilirubin UDP-Glucuronosyltransferase in a Patient with Crigler-Najjar Syndrome Type II

✍ Scribed by S. Aono; Y. Yamada; H. Keino; N. Hanada; T. Nakagawa; Y. Sasaoka; T. Yazawa; H. Sato; O. Koiwai

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Analysis of bilirubin uridine 5′-diphosp

✍ Kazuo Yamamoto; Yoko Soeda; Toshinori Kamisako; Hiroo Hosaka; Miya Fukano; H. Sa 📂 Article 📅 1998 🏛 Nature Publishing Group 🌐 English ⚖ 277 KB

Identification of a novel deletion in UD

✍ Elísio Costa; Emília Vieira; Ana Isabel Lopes; Maria Joana Saldanha; Dora Brites 📂 Article 📅 2009 🏛 Elsevier Science 🌐 English ⚖ 377 KB

Bilirubin-UDP-glucuronosyltransferase: G

✍ Hiroshi Sato; Sachiko Aono; Olivier Darios; Jean Michel Heard; Osamu Koiwai 📂 Article 📅 1994 🏛 AlphaMed Press 🌐 English ⚖ 631 KB

Three Japanese patients with Crigler-Naj

✍ Osamu Koiwai; Yoshihiro Yasui; Kayo Hasada; Sachiko Aono; Hiroshi Sato; Morihiko 📂 Article 📅 1995 🏛 Nature Publishing Group 🌐 English ⚖ 391 KB

Sequence of exons and the flanking regio

✍ Piter J. Bosma; Namita Roy Chowdhury; Bart G. Goldhoorn; Martin H. Hofker; Ronal 📂 Article 📅 1992 🏛 John Wiley and Sons 🌐 English ⚖ 814 KB

Crigler-Najjar syndrome, type I is a heterogeneous

Analysis of the UDP-glucuronosyltransfer

✍ Elísio Costa; Emília Vieira; Marcia Martins; Jorge Saraiva; Eugénia Cancela; Mig 📂 Article 📅 2006 🏛 Elsevier Science 🌐 English ⚖ 294 KB