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Prenatal molecular diagnosis of severe ornithine carbamoyltransferase deficiency due to a novel mutation, E181G
Author(s) -
Topaloglu A. K.,
Sansaricq C.,
Fox J. E.,
Bale A. E.,
Tuchman M.,
Desnick R. J.
Publication year - 1999
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:1005411601985
Subject(s) - medical genetics , human genetics , medicine , genetics , biology , gene
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