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Type I hereditary tyrosinaemia: Presentation of 11 cases
Author(s) -
Coşkun T.,
Özalp İ.,
Koçak N.,
Yüce A.,
Çaglar M.,
Berger R.
Publication year - 1991
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/bf01799947
Subject(s) - tyrosinemia , presentation (obstetrics) , human genetics , medicine , metabolic disease , pediatrics , chemistry , genetics , biology , surgery , biochemistry , gene , tyrosine
Summary Diagnostic information is supplied for the early detection of subacute and chronic forms of type I tyrosinaemia.
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