Phenylketonuria missense mutations in the Mediterranean
- 1 January 1991
- Vol. 9 (1) , 96-103
- https://doi.org/10.1016/0888-7543(91)90225-4
Abstract
No abstract availableKeywords
This publication has 23 references indexed in Scilit:
- Haplotype distribution and molecular defects of PKU in ItalyJournal of Inherited Metabolic Disease, 1990
- A single origin of phenylketonuria in Yemenite JewsNature, 1990
- CpG dinucleotides are mutation hot spots in phenylketonuriaGenomics, 1989
- Phenylketonuria: distribution of DNA diagnostic patterns in German familiesHuman Genetics, 1988
- The CpG dinucleotide and human genetic diseaseHuman Genetics, 1988
- Polymorphic DNA haplotypes at the human phenylalanine hydroxylase locus and their relationship with phenylketonuriaHuman Genetics, 1987
- An ammo-acid substitution involved in phenylketonuria is in linkage disequilibrium with DNA haplotype 2Nature, 1987
- Electroporation for the efficient transfection of mammalian cells with DNANucleic Acids Research, 1987
- Tight linkage between a splicing mutation and a specific DNA haplotype in phenylketonuriaNature, 1986
- POLYMORPHIC DNA HAPLOTYPES AT THE PHENYLALANINE HYDROXYLASE LOCUS IN PRENATAL DIAGNOSIS OF PHENYLKETONURIAThe Lancet, 1986