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Ngu, L. H.
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Ngu, L. H.
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Ngu, L. H.
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Mutation Study of Malaysian Patients with Ornithine Transcarbamylase Deficiency: Clinical, Molecular, and Bioinformatics Analyses of Two Novel Missense Mutations of the OTC Gene
by
Ali, E.Z
,
Jusoh, S.A
,
Mohd Radzi, M.A
,
Ngu
,
L.H
,
Zakaria, Y.
Published 2018
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Article
2
{}
by
Omoregie, A. I.
,
Senian, N.
,
Phua, Y. L.
,
Ngu
,
L
.
H
.
,
Ong, D. E. L.
,
Ginjom, I. R. H.
,
Nissom, P. M.
Published 2016-01-01
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Related Subjects
Article
Computational Biology
Female
Humans
Infant, Newborn
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Molecular Docking Simulation
Mutation
Mutation, Missense
Ornithine Carbamoyltransferase Deficiency Disease
adolescent
adult
ammonia
arginine
bioinformatics
biology
catalysis
child
citrulline
clinical article
clinical assessment
cohort analysis
comparative study
computer model
conformational transition
controlled study
female
genetic analysis
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