Novel initiation codon mutation Met1Thr identified in a patient with partial hypoxanthine-guanine phosphoribosyl-transferase (HPRT) deficiency: HPRT Heidelberg

✍ Scribed by Birgit S. Gathof; Jan Geissler; Anne M. Wingen; Ursula Gresser

• Publisher: John Wiley and Sons
• Year: 1996
• Tongue: English
• Weight: 108 KB
• Volume: 7
• Category: Article
• ISSN: 1059-7794
• DOI: 10.1002/(sici)1098-1004(1996)7:2<184::aid-humu21>3.0.co;2-y