Premium Prenatal molecular diagnosis of severe ornithine carbamoyltransferase deficiency due to a novel mutation, E181GPremium
Author(s)
Topaloglu A. K.,
Sansaricq C.,
Fox J. E.,
Bale A. E.,
Tuchman M.,
Desnick R. J.
Publication year1999
Publication title
journal of inherited metabolic disease
Resource typeJournals
PublisherKluwer Academic Publishers
Subject(s)biology , gene , genetics , human genetics , medical genetics , medicine
Language(s)English
SCImago Journal Rank1.462
H-Index102
eISSN1573-2665
pISSN0141-8955
DOI10.1023/a:1005411601985
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