![](/img/cover-not-exists.png)
Novel initiation codon mutation Met1Thr identified in a patient with partial hypoxanthine-guanine phosphoribosyl-transferase (HPRT) deficiency: HPRT Heidelberg
Birgit S. Gathof, Jan Geissler, Anne M. Wingen, Ursula GresserVolume:
7
Year:
1996
Language:
english
Pages:
1
DOI:
10.1002/(sici)1098-1004(1996)7:23.0.co;2-y
File:
PDF, 108 KB
english, 1996