Molecular Analysis of Mutations in the Human HPRT Gene
Author:
Publisher
Springer US
Link
http://link.springer.com/content/pdf/10.1007/978-1-0716-0223-2_20
Reference55 articles.
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2. Patel PI, Yang TP, Stout JT, Konecki DS, Chinault AC, Caskey CT (1986) Mutational diversity at the human HPRT locus. Prog Clin Biol Res 209A:457–463
3. Stout JT, Caskey CT (1988) The Lesch-Nyhan syndrome: clinical, molecular and genetic aspects. Trends Genet 4:175–178
4. Jinnah HA, De Gregorio L, Harris JC, Nyhan WL, O’Neill JP (2000) The spectrum of inherited mutations causing HPRT deficiency: 75 new cases and a review of 196 previously reported cases. Mutat Res 463:309–326
5. Szybalski W (1959) Genetics of human cell lines. II. Methods or determination of mutation rates to drug resistance. Exp Cell Res 18:588–591
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