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Year | Number of Results |
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2013 | 1 |
2016 | 2 |
2024 | 0 |
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Adaptor proteins MiD49 and MiD51 can act independently of Mff and Fis1 in Drp1 recruitment and are specific for mitochondrial fission.
J Biol Chem. 2013 Sep 20;288(38):27584-27593. doi: 10.1074/jbc.M113.479873. Epub 2013 Aug 6.
J Biol Chem. 2013.
PMID: 23921378
Free PMC article.
Postnatal microcephaly and pain insensitivity due to a de novo heterozygous DNM1L mutation causing impaired mitochondrial fission and function.
Sheffer R, Douiev L, Edvardson S, Shaag A, Tamimi K, Soiferman D, Meiner V, Saada A.
Sheffer R, et al.
Am J Med Genet A. 2016 Jun;170(6):1603-7. doi: 10.1002/ajmg.a.37624. Epub 2016 Mar 17.
Am J Med Genet A. 2016.
PMID: 26992161
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A novel de novo dominant negative mutation in DNM1L impairs mitochondrial fission and presents as childhood epileptic encephalopathy.
Fahrner JA, Liu R, Perry MS, Klein J, Chan DC.
Fahrner JA, et al.
Am J Med Genet A. 2016 Aug;170(8):2002-11. doi: 10.1002/ajmg.a.37721. Epub 2016 May 4.
Am J Med Genet A. 2016.
PMID: 27145208
Free PMC article.
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