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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
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PubMed (GeneRIF) for id: 4540

55 results

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Page 1
Whole-exome sequencing reveals a novel mutation of MT-ND5 gene in a mitochondrial cardiomyopathy pedigree: Patients who show biventricular hypertrophy, hyperlactacidemia, pulmonary hypertension, and decreased exercise tolerance.
Zhou N, Tang L, Jiang Y, Qin S, Cui J, Wang Y, Zhu W, Zhao W, Pan C, Shu X. Zhou N, et al. Anatol J Cardiol. 2019 Jan;21(1):18-24. doi: 10.14744/AnatolJCardiol.2018.53258. Anatol J Cardiol. 2019. PMID: 30587702 Free PMC article.
MT-ND5 Mutation Exhibits Highly Variable Neurological Manifestations at Low Mutant Load.
Ng YS, Lax NZ, Maddison P, Alston CL, Blakely EL, Hepplewhite PD, Riordan G, Meldau S, Chinnery PF, Pierre G, Chronopoulou E, Du A, Hughes I, Morris AA, Kamakari S, Chrousos G, Rodenburg RJ, Saris CGJ, Feeney C, Hardy SA, Sakakibara T, Sudo A, Okazaki Y, Murayama K, Mundy H, Hanna MG, Ohtake A, Schaefer AM, Champion MP, Turnbull DM, Taylor RW, Pitceathly RDS, McFarland R, Gorman GS. Ng YS, et al. EBioMedicine. 2018 Apr;30:86-93. doi: 10.1016/j.ebiom.2018.02.010. Epub 2018 Feb 24. EBioMedicine. 2018. PMID: 29506874 Free PMC article.
Whole mitochondrial genome screening of a family with maternally inherited diabetes and deafness (MIDD) associated with retinopathy: A putative haplotype associated to MIDD and a novel MT-CO2 m.8241T>G mutation.
Tabebi M, Charfi N, Kallabi F, Alila-Fersi O, Ben Mahmoud A, Tlili A, Keskes-Ammar L, Kamoun H, Abid M, Mnif M, Fakhfakh F. Tabebi M, et al. J Diabetes Complications. 2017 Jan;31(1):253-259. doi: 10.1016/j.jdiacomp.2016.06.028. Epub 2016 Jul 1. J Diabetes Complications. 2017. PMID: 27422531
55 results