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Relation between phenylalanine hydroxylase genotypes and phenotypic parameters of diagnosis and treatment of hyperphenylalaninaemic disorders
Author(s) -
LichterKonecki U.,
Rupp A.,
Konecki D. S.,
Trefz F. K.,
Schmidt H.,
Burgard P.
Publication year - 1994
Publication title -
journal of inherited metabolic disease
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.462
H-Index - 102
eISSN - 1573-2665
pISSN - 0141-8955
DOI - 10.1007/bf00711831
Subject(s) - german , university hospital , medicine , phenylalanine hydroxylase , pediatrics , family medicine , phenylalanine , genetics , biology , philosophy , linguistics , amino acid