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SHORT REPORT: Pitfalls in the detection of heterozygosity by allopurinol in a variant form of ornithine carbamoyltransferase deficiency
Author(s) -
Barshop B. A.,
Nyhan W. L.,
Climent C.,
Rubio V.
Publication year - 2001
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:1010593916546
Subject(s) - valencia , molecular genetics , medicine , genetics , biology , gene , ecology