Mutations in MTFMT underlie a human disorder of formylation causing impaired mitochondrial translation

Tucker, Elena J, Hershman, Steven G, Köhrer, Caroline, Belcher-Timme, Casey A, Patel, Jinal, Goldberger, Olga A, Christodoulou, John, Silberstein, Jonathon M, McKenzie, Matthew, Ryan, Michael T, Compton, Alison G, Jaffe, Jacob D, Carr, Steven A, Calvo, Sarah E, RajBhandary, Uttam L, Thorburn, David R and Mootha, Vamsi K 2011, Mutations in MTFMT underlie a human disorder of formylation causing impaired mitochondrial translation, Cell metabolism, vol. 14, no. 3, pp. 428-434, doi: 10.1016/j.cmet.2011.07.010.

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Title Mutations in MTFMT underlie a human disorder of formylation causing impaired mitochondrial translation
Author(s) Tucker, Elena J
Hershman, Steven G
Köhrer, Caroline
Belcher-Timme, Casey A
Patel, Jinal
Goldberger, Olga A
Christodoulou, John
Silberstein, Jonathon M
McKenzie, MatthewORCID iD for McKenzie, Matthew orcid.org/0000-0001-7508-1800
Ryan, Michael T
Compton, Alison G
Jaffe, Jacob D
Carr, Steven A
Calvo, Sarah E
RajBhandary, Uttam L
Thorburn, David R
Mootha, Vamsi K
Journal name Cell metabolism
Volume number 14
Issue number 3
Start page 428
End page 434
Total pages 7
Publisher Elsevier
Place of publication Amsterdam, The Netherlands
Publication date 2011-09-07
ISSN 1550-4131
1932-7420
Keyword(s) cells, cultured
child
cyclooxygenase 1
DNA, mitochondrial
fibroblasts
heterozygote
hydroxymethyl and formyl transferases
immunoblotting
Leigh disease
lentivirus
mitochondria
mitochondrial proteins
mutation
protein biosynthesis
RNA, transfer, met
sequence analysis, DNA
transduction, genetic
virion
science & technology
life sciences & biomedicine
cell biology
endocrinology & metabolism
Language eng
DOI 10.1016/j.cmet.2011.07.010
Field of Research 0601 Biochemistry And Cell Biology
1101 Medical Biochemistry And Metabolomics
Copyright notice ©2011, Elsevier Inc.
Persistent URL http://hdl.handle.net/10536/DRO/DU:30112396

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