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 J; Journal Of Medical Genetics, 1991, vol. 28, issue 10, p 686, ISSN 00222593. ISBN 00222593.

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