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Phenylalanine hydroxylase deficiency in a population in Germany: Mutational profile and nine novel mutations
Author(s) -
Guldberg Per,
Mallmann Rudolf,
Henriksen Karen Friis,
Güttler Flemming
Publication year - 1996
Publication title -
human mutation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.981
H-Index - 162
eISSN - 1098-1004
pISSN - 1059-7794
DOI - 10.1002/(sici)1098-1004(1996)8:3<276::aid-humu14>3.0.co;2-#
Subject(s) - biology , phenylalanine hydroxylase , genetics , mutation , population , 21 hydroxylase , phenylalanine , gene , demography , amino acid , sociology