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

Hershman, Steven G; Tucker, Elena J; Koehrer, Caroline; Belcher-Timme, Casey A; Patel, Jinal; Goldberger, Olga A; Christodoulou, John; Silberstein, Jonathon M; McKenzie, Matthew; Ryan, Michael T; Compton, Alison G; Garone, Caterina; Garcia-Diaz, Beatriz; DiMauro, Salvatore; Jaffe, Jacob D; Carr, Steven A; Calvo, Sarah E; RajBhandary, Uttam L; Thorburn, David R; Mootha, Vamsi K

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

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posted on 2022-11-23, 05:04 authored by Steven G Hershman, Elena J Tucker, Caroline Koehrer, Casey A Belcher-Timme, Jinal Patel, Olga A Goldberger, John Christodoulou, Jonathon M Silberstein, Matthew McKenzieMatthew McKenzie, Michael T Ryan, Alison G Compton, Caterina Garone, Beatriz Garcia-Diaz, Salvatore DiMauro, Jacob D Jaffe, Steven A Carr, Sarah E Calvo, Uttam L RajBhandary, David R Thorburn, Vamsi K Mootha

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

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DOI - Is version of https://doi.org/10.1016/j.mito.2012.07.084

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English

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https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000309023700092&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=a045e4b2bb1f2b747c68c720ec8913b7

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E3.1 Extract of paper

Volume

12

Pagination

583-583

ISSN

1567-7249

Title of proceedings

MITOCHONDRION

Issue

5

Publisher

ELSEVIER SCI LTD

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Science & Technology Life Sciences & Biomedicine Cell Biology Genetics & Heredity

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

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