Insights into the Mutation-Induced HHH Syndrome from Modeling Human Mitochondrial Ornithine Transporter-1-Reference-Cited by-同舟云学术

Insights into the Mutation-Induced HHH Syndrome from Modeling Human Mitochondrial Ornithine Transporter-1

Published:2012-01-26 Issue:1 Volume:7 Page:e31048
ISSN:1932-6203
Container-title:PLoS ONE
language:en
Short-container-title:PLoS ONE

Author:

Wang Jing-Fang,Chou Kuo-Chen

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference65 articles.

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2. Studies on a case of HHH-syndrome (hyperammonemia, hyperornithinemia, homocitrullinuria).;FA Hommes;Neuropediatrics,1986

3. A case of hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome with spastic paraparesis and severe distal muscle atrophy of lower limbs.;H Shigeto;Rinsho Shinkeigaku,1992

4. Anesthesia for a patient with the hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome.;R Noguchi;Masui,1988

5. Abnormal urinary excretion of polyamines in HHH syndrome (hyperornithinemia associated with hyperammonemia and homocitrullinuria).;H Shimizu;Brain Dev,1990

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