Avigad S.,1987

Avigad S., Cohen B.E., Woo S.L.C., Shiloh Y. A specific deletion within the phenylalanine hydroxylase gene is common most Yemenit Jewish phenylketonuria patients. - Am.J.Hum.Genet., 1987, v. 41, p. A205.

Смотрите также:

ФКУ, мутации гена ФАГ