Simple detection of a (Finnish) hereditary tyrosinemia type 1 mutation.

St-Louis, M

Simple detection of a (Finnish) hereditary tyrosinemia type 1 mutation. [electronic resource] - Human mutation 1996 - 379-80 p. digital

Publication Type: Letter; Research Support, Non-U.S. Gov't

1059-7794

10.1002/(SICI)1098-1004(1996)7:4<379::AID-HUMU20>3.0.CO;2-Z doi


Amino Acid Metabolism, Inborn Errors--ethnology
Base Sequence
DNA Primers
Finland
Genetic Carrier Screening
Heterozygote
Humans
Molecular Sequence Data
Mutation
Tyrosine--blood