Mutation or knock-down of 17β-hydroxysteroid dehydrogenase type 10 cause loss of MRPP1 and impaired processing of mitochondrial heavy strand transcripts.

Site
Pubmed id
24549042
Authors

Deutschmann AJ, Amberger A, Zavadil C, Steinbeisser H, Mayr JA, Feichtinger RG, Oerum S, Yue WW, Zschocke J

DOI
10.1093/hmg/ddu072
Journal
Hum. Mol. Genet.
Publication Date
2014-2-26
Year
2014
N Publication Date
Validated
Y