TY  - GEN
AU  - Scriver,C R
AU  - Clow,C L
TI  - Phenylketonuria and other phenylalanine hydroxylation mutants in man
SN  - 0066-4197
PY  - 1981///0526
KW  - Alleles
KW  - Amino Acid Metabolism, Inborn Errors
KW  - diagnosis
KW  - Animals
KW  - Biopterins
KW  - analogs & derivatives
KW  - Dihydropteridine Reductase
KW  - genetics
KW  - Female
KW  - Fetal Diseases
KW  - etiology
KW  - Gene Frequency
KW  - Genetic Carrier Screening
KW  - Heterozygote
KW  - Humans
KW  - Hydroxylation
KW  - Phenylalanine
KW  - metabolism
KW  - Phenylalanine Hydroxylase
KW  - deficiency
KW  - Phenylketonurias
KW  - diet therapy
KW  - Pregnancy
KW  - Pregnancy Complications
KW  - Rats
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Review
UR  - https://doi.org/10.1146/annurev.ge.14.120180.001143
ER  -