Fatigue and quality of life in citrin deficiency during adaptation and compensation stage-Reference-Cited by-同舟云学术

Fatigue and quality of life in citrin deficiency during adaptation and compensation stage

Published:2013-05 Issue:1 Volume:109 Page:9-13
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

Okano Yoshiyuki,Kobayashi Kyoko,Ihara Kenji,Ito Tetsuya,Yoshino Makoto,Watanabe Yoriko,Kaji Shunsaku,Ohura Toshihiro,Nagao Masayoshi,Noguchi Atsuko,Mushiake Sotaro,Hohashi Naohiro,Hashimoto-Tamaoki Tomoko

Funder

Ministry of Education, Culture, Sports, Science, and Technology of Japan

Ministry of Health, Labor and Welfare of Japan

Suyama Research Foundation

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference41 articles.

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2. Citrin and aralar1 are Ca(2+) stimulated aspartate/glutamate transporters in mitochondria;Palmieri;EMBO J.,2001

3. Diseases caused by defects of mitochondrial carriers;Palmieri;Biochim. Biophys. Acta,2008

4. Mitochondrial aspartate glutamate carrier (citrin) deficiency as the cause of adult-onset type II citrullinemia (CTLN2) and idiopathic neonatal hepatitis (NICCD);Saheki;J. Hum. Genet.,2002

5. Screening of SLC25A13 mutations in early and late onset patients with citrin deficiency and in the Japanese population: identification of two novel mutations and establishment of multiple DNA diagnosis method for nine mutations;Yamaguchi;Hum. Mutat.,2002

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