High prevalence of the H1069Q mutation in East German patients with Wilson disease: rapid detection of mutations by limited sequencing and phenotype–genotype analysis

✍ Scribed by Karel Caca; Peter Ferenci; Hans-Jürgen Kühn; Claudia Polli; Helmut Willgerodt; Bernhard Kunath; Wieland Hermann; Joachim Mössner; Frieder Berr

• Book ID: 119526733
• Publisher: Elsevier Science
• Year: 2001
• Tongue: English
• Weight: 144 KB
• Volume: 35
• Category: Article
• ISSN: 0168-8278
• DOI: 10.1016/s0168-8278(01)00219-7