Rare recessive loss-of-function methionyl-tRNA synthetase mutations presenting as a multi-organ phenotype

Authors

Eline van Meel, Washington University School of Medicine in St. Louis
Daniel J. Wegner, Washington University School of Medicine in St. Louis
Paul Cliften, Washington University School of Medicine in St. Louis
Marcia C. Willing, Washington University School of Medicine in St. Louis
Frances V. White, Washington University School of Medicine in St. Louis
Stuart Kornfeld, Washington University School of Medicine in St. LouisFollow
F. Sessions Cole, Washington University School of Medicine in St. Louis

Journal

BMC Medical Genetics

Publication Date

2013

Volume

14

Inclusive Pages

106

Document Type

Open Access Publication

Rights and Permissions

van Meel et al. BMC Medical Genetics 2013, 14:106 http://www.biomedcentral.com/1471-2350/14/106

Recommended Citation

van Meel, Eline; Wegner, Daniel J.; Cliften, Paul; Willing, Marcia C.; White, Frances V.; Kornfeld, Stuart; and Cole, F. Sessions, "Rare recessive loss-of-function methionyl-tRNA synthetase mutations presenting as a multi-organ phenotype." BMC Medical Genetics. 14, 106. (2013).
https://digitalcommons.wustl.edu/open_access_pubs/1677