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Large deletions in the phenylalanine hydroxylase gene as a cause of phenylketonuria in India
Author(s) -
Guldberg P.,
Henriksen K. F.,
Mammen K. C.,
Levy H. L.,
Güttler F.
Publication year - 1997
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 - 10.1023/a:1005352725283
Subject(s) - metabolic disease , biochemistry , medicine