Lichter-Konecki U.,1988a

Lichter-Konecki U., Konecki D.S., DiLella A.G., Brayton K., Marvit J., Hahn T.M., Trefz F.K., Woo S.L.C. Phenyl- alanine hydroxylase deficiency caused by a single base substitu- tion in an exon of the human phenylalanine hydroxylase gene. - Biochemistry, 1988, v. 27, p. 2881-2885.

Смотрите также:

ФКУ, мутации гена ФАГ

Табл. 4 pat