Cite
HARVARD Citation
Kalaydjieva, L. et al. (1991). Silent mutations in the phenylalanine hydroxylase gene as an aid to the diagnosis of phenylketonuria.. Journal of medical genetics. 28 (10), pp. 686-690. [Online].
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Kalaydjieva, L. et al. (1991). Silent mutations in the phenylalanine hydroxylase gene as an aid to the diagnosis of phenylketonuria.. Journal of medical genetics. 28 (10), pp. 686-690. [Online].