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Publication
PropertyValue
Working Groups Meitinger
SubprojectNone
Open AccessOpen Access Yes
Publication TypeJournal Article
Peer ReviewedYes
PMIDPubMed ID 25434004
DOIDOI 10.1016/j.ajhg.2014.10.017
Publication Year2014
TitleMutations in GTPBP3 cause a mitochondrial translation defect associated with hypertrophic cardiomyopathy, lactic acidosis, and encephalopathy. Wikidata
JournalAmerican journal of human genetics
ISSN0002-9297
ESSN1537-6605
URL https://www.ncbi.nlm.nih.gov/pubmed/?term=25434004%5Buid%5D
Pages708-20
Issue6
Volume95
Journal AbbreviationAm J Hum Genet
AuthorsKopajtich R, Nicholls TJ, Rorbach J, Metodiev MD, Freisinger P, Mandel H, Vanlander A, Ghezzi D, Carrozzo R, Taylor RW, Marquard K, Murayama K, Wieland T, Schwarzmayr T, Mayr JA, Pearce SF, Powell CA, Saada A, Ohtake A, Invernizzi F, Lamantea E, Sommerville EW, Pyle A, Chinnery PF, Crushell E, Okazaki Y, Kohda M, Kishita Y, Tokuzawa Y, Assouline Z, Rio M, Feillet F, Mousson de Camaret B, Chretien D, Munnich A, Menten B, Sante T, Smet J, Régal L, Lorber A, Khoury A, Zeviani M, Strom TM, Meitinger T, Bertini ES, Van Coster R, Klopstock T, Rötig A, Haack TB, Minczuk M, Prokisch H
First AuthorKopajtich R
Last AuthorProkisch H
ScholiaScholia Wikidata-based representation at Scholia

 External Resources

 Q34450113  Wikidata ID