Novel intragenic deletions and point mutations of the ornithine transcarbamylase gene in congenital hyperammonemia
Open Access
- 1 January 1998
- journal article
- case report
- Published by Hindawi Limited in Human Mutation
- Vol. 11 (S1) , S81-S84
- https://doi.org/10.1002/humu.1380110128
Abstract
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