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Keyword [Urea Cycle Disorder]
Result: 1 - 3 | Page: 1 of 1
1.
Two Cases Of Congenital Hyperammonemia
2.
Clinicaland Mutation Analyses Of 11 Cases With Late-onset Ornithine Transcarbamylase Deficiency
3.
Clinical Characteristics,mutation Analysis And The Establishment Of IPS Cells Line With Liver Organoid Derived From Peripheral Blood Mononuclear Cells Of Urea Cycle Disorder Patients
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