Author:
Eiken Hans Geir,Stangeland Karin,Skjelkvålez Leif,Knappskog Per M.,Boman Helge,Apold Jaran
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Reference21 articles.
1. Abadie V, Lyonnet S, Maurin N, Berthelon M, Caillaud C, Giraud F, Mattei J-F et al (1989) CpG dinucleotides are mutation hot spots in phenylketonuria. Genomics 5:936–939
2. Apold J, Eiken HG, Odland E, Fredriksen Å, Bakken A, Lorens JB, Boman H (1990) A termination mutation prevalent in Norwegian haplotype 7 phenylketonuria genes. Am J Hum Genet 47:1002–1007
3. Daiger SP, Chakraborty R, Reed L, Fekete G, Schuler D, Berenssi G, Nasz I et al (1989) Polymorphic DNA haplotypes at the phenylalanine hydroxylase (PAH) locus in European families with phenylketonuria (PKU). Am J Hum Genet 45:319–324
4. DiLella AG, Marvit J, Lidsky AS, Guttler F, Woo SLC (1986) Tight linkage between a splicing mutation and a specific DNA haplotype in phenylketonuria. Nature 322:799–803
5. DiLella AG, Marvit J, Brayton K, Woo SLC (1987) An amino acid substitution involved in phenylketonuria is in linkage disequilibrium with DNA haplotype 2. Nature 327:333–336
Cited by
17 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献