PubMed for id: 374115

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1979	1
1992	1
2016	1
2019	1
2020	1
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Page 1

A PRIMPOL mutation and variants in multiple genes may contribute to phenotypes in a familial case with chronic progressive external ophthalmoplegia symptoms.

Kasamo K, Nakamura M, Daimou Y, Sano A. Kasamo K, et al. Neurosci Res. 2020 Aug;157:58-63. doi: 10.1016/j.neures.2019.07.006. Epub 2019 Jul 23. Neurosci Res. 2020. PMID: 31348995

Functional characterization of orbicularis oculi and extraocular muscles.

Sekulic-Jablanovic M, Ullrich ND, Goldblum D, Palmowski-Wolfe A, Zorzato F, Treves S. Sekulic-Jablanovic M, et al. J Gen Physiol. 2016 May;147(5):395-406. doi: 10.1085/jgp.201511542. Epub 2016 Apr 11. J Gen Physiol. 2016. PMID: 27069119 Free PMC article.

Diagnostic value of ophthalmologic findings in myotonic dystrophy: comparison with risks calculated by haplotype analysis of closely linked restriction fragment length polymorphisms.

Ashizawa T, Hejtmancik JF, Liu J, Perryman MB, Epstein HF, Koch DD. Ashizawa T, et al. Am J Med Genet. 1992 Jan 1;42(1):55-60. doi: 10.1002/ajmg.1320420113. Am J Med Genet. 1992. PMID: 1364051

A familial mitochondrial myopathy with central defect in neural transmission.

Barron SA, Heffner RR Jr, Zwirecki R. Barron SA, et al. Arch Neurol. 1979 Sep;36(9):553-6. doi: 10.1001/archneur.1979.00500450047007. Arch Neurol. 1979. PMID: 224846

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