Mutation Study of Malaysian Patients with Ornithine Transcarbamylase Deficiency: Clinical, Molecular, and Bioinformatics Analyses of Two Novel Missense Mutations of the OTC Gene
Ornithine transcarbamylase deficiency (OTCD), an X-linked disorder that results from mutations in the OTC gene, causes hyperammonemia and leads to various clinical manifestations. Mutations occurring close to the catalytic site of OTCase can cause severe OTCD phenotypes compared with those caused by...
| Published in: | BioMed Research International |
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| Main Author: | |
| Format: | Article |
| Language: | English |
| Published: |
Hindawi Limited
2018
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| Online Access: | https://www.scopus.com/inward/record.uri?eid=2-s2.0-85053057002&doi=10.1155%2f2018%2f4320831&partnerID=40&md5=ade86663fa9db435bf44cb36e7ac8c81 |