Lyonnet S.,1989

Lyonnet S., Caillaud C., Rey F., Berthelon M., Frezal J., Rey J., Munnich A. Molecular genetics of phenylketonuria in Medi- terranean countries: a mutation associated with partial phenylala- nine hydroxylase deficiency. - Am.J.Hum.Genet., 1989, v. 44, p.511- 517.

Смотрите также:

ФКУ, мутации гена ФАГ

Табл. 4 pat