Mutational spectrum of phenylalanine hydroxylase deficiency in Sicily: implications for diagnosis of hyperphenyl-alaninemia in Southern Europe-Reference-Cited by-同舟云学术

Mutational spectrum of phenylalanine hydroxylase deficiency in Sicily: implications for diagnosis of hyperphenyl-alaninemia in Southern Europe

Published:1993 Issue:10 Volume:2 Page:1703-1707
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Hum Mol Genet

Author:

Guldberg Per,Romano Valentino,Ceratto Nadia,Bosco Paolo,Cluna Marina,Indellcato Anna,Mollica Florindo,Mell Cettina,Glovannini Marcello,Riva Enrica,Biasuccl Glacomo,Henriksen Karen Frils,Güttler Flemming

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/2/10/1703/1787391/2-10-1703.pdf

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