Mutational and phenotypical spectrum of phenylalanine hydroxylase deficiency in Denmark
Bayat, Allan, Yasmeen, Saiqa, Lund, Allan, Nielsen, Jytte Bieber, Møller, Lisbeth BirkLanguage:
english
Journal:
Clinical Genetics
DOI:
10.1111/cge.12692
Date:
November, 2015
File:
PDF, 122 KB
english, 2015