๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Missense mutations at the FKBP12-rapamycin-binding site of TOR1

โœ Scribed by Katie Freeman; George P. Livi


Book ID
116133655
Publisher
Elsevier Science
Year
1996
Tongue
English
Weight
651 KB
Volume
172
Category
Article
ISSN
0378-1119

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


A germ line mutation within the coding s
โœ Shin Fujimori; Tetsuo Tagaya; Naoyuki Kamatani; Ieo Akaoka ๐Ÿ“‚ Article ๐Ÿ“… 1992 ๐Ÿ› Springer ๐ŸŒ English โš– 529 KB

Lesch-Nyhan syndrome caused by a complete deficiency of hypoxanthine guanine phosphoribosyltransferase (HPRT) is the result of a heterogeneous group of germ line mutations. Identification of each mutant gene provides valuable information as to the type of mutation that occurs spontaneously. We repor