Structure–function analyses of the G729R 2-oxoadipate dehydrogenase genetic variant associated with a disorder of l-lysine metabolism-Reference-Cited by-同舟云学术

Structure–function analyses of the G729R 2-oxoadipate dehydrogenase genetic variant associated with a disorder of l-lysine metabolism

Published:2020-06 Issue:23 Volume:295 Page:8078-8095
ISSN:0021-9258
Container-title:Journal of Biological Chemistry
language:en
Short-container-title:Journal of Biological Chemistry

Author:

Zhang Xu,Nemeria Natalia S.,Leandro João,Houten Sander^ORCID,Lazarus Michael^ORCID,Gerfen Gary,Ozohanics Oliver,Ambrus Attila^ORCID,Nagy Balint^ORCID,Brukh Roman,Jordan Frank^ORCID

Funder

HHS | National Institutes of Health

National Science Foundation

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry

Reference54 articles.

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3. Genetic basis of α-aminoadipic and α-ketoadipic aciduria;Hagen;J. Inherit. Metab. Dis,2015

4. A nonsense mutation in DHTKD1 causes Charcot-Marie-Tooth type 2 in a large Chinese pedigree;Xu;Am. J. Hum. Genet,2012

5. DHTKD1 is essential for mitochondrial biogenesis and function maintenance;Xu;FEBS Lett,2013

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