Institutional members access full text with Ovid®

Share this article on:

A novel compound heterozygous variation of the uridine-diphosphoglucuronosyl transferase 1A 1 gene that causes Crigler–Najjar syndrome type II

Huang, Ching-Shana,b; Luo, Guo-Anb; Huang, May-Jena; Chen, En-Sunga; Young, Ton-Hoc; Chao, You-Chend

Pharmacogenetics and Genomics: October 2001 - Volume 11 - Issue 7 - p 639-642
Short Communication

aDepartment of Laboratory Medicine, Cathay General Hospital, Taipei, Taiwan, bDepartment of Chemistry, Tsinghua University, Beijing, China, cDepartment of Internal Medicine, Cardinal Tien Hospital, Taipei, Taiwan and dDepartment of Internal Medicine, Tri-Service General Hospital, Taipei, Taiwan

Received 3 November 2000; accepted 31 January 2001

Correspondence to Ching-Shan Huang, Department of Laboratory Medicine, Cathay General Hospital, 280 sec 4, Jen-Ai Road, Taipei, 106 Taiwan Tel/fax: +886 2 270 25104; e-mail: pcsh@ms1.cgh.org.tw

© 2001 Lippincott Williams & Wilkins, Inc.