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Management of manifesting FOXRED1 carriers is complex.
Finsterer J, Zarrouk-Mahjoub S. Finsterer J, et al. Among authors: zarrouk mahjoub s. Mol Genet Metab Rep. 2019 Feb 23;19:100463. doi: 10.1016/j.ymgmr.2019.100463. eCollection 2019 Jun. Mol Genet Metab Rep. 2019. PMID: 31193306 Free PMC article. No abstract available.
MELAS syndrome due to the m.3291T > C mutation.
Finsterer J, Zarrouk-Mahjoub S. Finsterer J, et al. Mol Genet Metab Rep. 2016 Apr 13;7:50. doi: 10.1016/j.ymgmr.2016.03.011. eCollection 2016 Jun. Mol Genet Metab Rep. 2016. PMID: 27134825 Free PMC article. No abstract available.
Arrhythmias in MELAS syndrome.
Finsterer J, Zarrouk-Mahjoub S. Finsterer J, et al. Mol Genet Metab Rep. 2016 Apr 14;7:54. doi: 10.1016/j.ymgmr.2016.03.008. eCollection 2016 Jun. Mol Genet Metab Rep. 2016. PMID: 27134827 Free PMC article. No abstract available.
Phenotypic heterogeneity of MELAS.
Finsterer J, Zarrouk-Mahjoub S. Finsterer J, et al. Mol Genet Metab Rep. 2016 Dec 11;10:18-19. doi: 10.1016/j.ymgmr.2016.12.002. eCollection 2017 Mar. Mol Genet Metab Rep. 2016. PMID: 27995078 Free PMC article. No abstract available.
204 results