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Phenylalanine hydroxylase deficiency exhibits mutation heterogeneity in two large old order Amish settlements
Author(s) -
Wang Heng,
Nye Leah,
Puffenberger Erik,
Morton Holmes
Publication year - 2007
Publication title -
american journal of medical genetics part a
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.064
H-Index - 112
eISSN - 1552-4833
pISSN - 1552-4825
DOI - 10.1002/ajmg.a.31852
Subject(s) - order (exchange) , special needs , pediatrics , medicine , library science , family medicine , gerontology , psychiatry , computer science , finance , economics
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