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A 22‐bp deletion in the phenylalanine hydroxylase gene causing phenylketonuria in an Arab family
Author(s) -
Kleiman Sandra,
Schwartz Gerard,
Woo Savio L. C.,
Shiloh Yosef
Publication year - 1992
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/humu.1380010414
Subject(s) - phenylalanine hydroxylase , biology , phenylalanine , gene , genetics , amino acid
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