Mitochondrial transporters of the SLC25 family and associated diseases: a review
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/s10545-014-9708-5
Reference57 articles.
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3. Camacho JA, Obie C, Biery B et al (1999) Hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome is caused by mutations in a gene encoding a mitochondrial ornithine transporter. Nat Genet 22:151–158
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