Human APRT deficiency: Indication for multiple origins of the most common Caucasian mutation and detection of a novel type of mutation involving intrastrand-templated repair

✍ Scribed by Claudia Menardi; Rainer Schneider; Felizia Neuschmid-Kaspar; Helmut Klocker; Monica Hirsch-Kauffmann; Bernhard Auer; Manfred Schweiger

• Publisher: John Wiley and Sons
• Year: 1997
• Tongue: English
• Weight: 170 KB
• Volume: 10
• Category: Article
• ISSN: 1059-7794
• DOI: 10.1002/(sici)1098-1004(1997)10:3<251::aid-humu15>3.0.co;2-z