Weinstein M.,1993
Weinstein M., Eisensmith R.C., Abadie V., Avigad S., Lyonnet S., Schwartz G., Munnich A., Woo S.L.C., Shiloh Y. A missense mutation, S349P, completely inactivates phenylalanine hydroxylase in north African Jews with phenylketonuria. - Hum.Genet., 1993, v. 90, p. 645-549.
