TY  - GEN
AU  - St-Louis,M
AU  - Poudrier,J
AU  - Tanguay,R M
TI  - Simple detection of a (Finnish) hereditary tyrosinemia type 1 mutation
SN  - 1059-7794
PY  - 1996///0927
KW  - Amino Acid Metabolism, Inborn Errors
KW  - ethnology
KW  - Base Sequence
KW  - DNA Primers
KW  - Finland
KW  - Genetic Carrier Screening
KW  - Heterozygote
KW  - Humans
KW  - Molecular Sequence Data
KW  - Mutation
KW  - Tyrosine
KW  - blood
N1  - Publication Type: Letter; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1002/(SICI)1098-1004(1996)7:4<379::AID-HUMU20>3.0.CO;2-Z
ER  -