Promoter analysis and transcriptional regulation of human carbonic anhydrase VIII gene in a MERRF disease cell model-Reference-Cited by-同舟云学术

Promoter analysis and transcriptional regulation of human carbonic anhydrase VIII gene in a MERRF disease cell model

Published:2018-03 Issue: Volume:641 Page:50-61
ISSN:0003-9861
Container-title:Archives of Biochemistry and Biophysics
language:en
Short-container-title:Archives of Biochemistry and Biophysics

Author:

Lo Che-Min,Ma Yi-Shing,Wei Yau-Huei,Hsieh Benjamin Y.T.,Hsieh Mingli

Funder

Ministry of Science and Technology of the Republic of China

Publisher

Elsevier BV

Subject

Molecular Biology,Biochemistry,Biophysics

Reference51 articles.

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3. A tRNA(Lys) mutation in the mtDNA is the causal genetic lesion underlying myoclonic epilepsy and ragged-red fiber (MERRF) syndrome;Noer;Am. J. Hum. Genet.,1991

4. Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation;Shoffner;Cell,1990

5. Gene dosage effect in one family with myoclonic epilepsy and ragged-red fibers (MERRF);Arpa;Acta Neurol. Scand.,1997

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