Clinical and biochemical characteristics of patients with ornithine transcarbamylase deficiency-Reference-Cited by-同舟云学术

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Clinical and biochemical characteristics of patients with ornithine transcarbamylase deficiency

Published:2020-10 Issue: Volume:84 Page:63-72
ISSN:0009-9120
Container-title:Clinical Biochemistry
language:en
Short-container-title:Clinical Biochemistry

Author:

Peng Min-Zhi,Li Xiu-Zhen,Mei Hui-Fen,Sheng Hui-Ying,Yin Xi,Jiang Min-Yan,Cai Yan-Na,Su Ling,Lin Yun-Ting,Shao Yong-Xian,Liu Li

Funder

National Natural Science Foundation of China

Publisher

Elsevier BV

Subject

Clinical Biochemistry,General Medicine

Reference37 articles.

1. Human ornithine transcarbamylase locus mapped to band xp21.1 near the duchenne muscular dystrophy locus;Lindgren;Science,1984

2. Long-term outcomes in ornithine transcarbamylase deficiency: A series of 90 patients;Brassier;Orphanet J Rare Dis,2015

3. Genotype-phenotype correlations in ornithine transcarbamylase deficiency: A mutation update;Caldovic;J Genet Genomics,2015

4. Effects of congenital hyperammonemia on the cerebral and hepatic levels of the intermediates of energy metabolism in spf mice;Ratnakumari;Biochem. Biophys. Res. Commun.,1992

5. Ammonia toxicity to the brain;Braissant;J. Inherit. Metab. Dis.,2013

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