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Silent mutations in the phenylalanine hydroxylase gene as an aid to the diagnosis of phenylketonuria.
Kalaydjieva, L, Dworniczak, B, Aulehla-Scholz, C, Devoto, M, Romeo, G, Sturhmann, M, Kucinskas, V, Yurgelyavicius, V, Horst, JVolume:
28
Language:
english
Journal:
Journal of Medical Genetics
DOI:
10.1136/jmg.28.10.686
Date:
October, 1991
File:
PDF, 787 KB
english, 1991