MYO1H is a novel candidate gene for autosomal dominant pure hereditary spastic paraplegia
Author:
Funder
Istanbul Teknik Üniversitesi
Publisher
Springer Science and Business Media LLC
Subject
Genetics,Molecular Biology,General Medicine
Link
https://link.springer.com/content/pdf/10.1007/s00438-022-01910-5.pdf
Reference46 articles.
1. Adams RJ, Pollard TD (1989) Binding of myosin I to membrane lipids. Nature 340:565–568. https://doi.org/10.1038/340565a0
2. Adzhubei IA, Schmidt S, Peshkin L et al (2010) A method and server for predicting damaging missense mutations. Nat Methods 7:248–249
3. Arun RM, Lakkakula BVKS, Chitharanjan AB (2016) Role of myosin 1H gene polymorphisms in mandibular retrognathism. Am J Orthod Dentofac Orthop 149:699–704. https://doi.org/10.1016/j.ajodo.2015.10.028
4. Bateman A, Martin MJ, Orchard S et al (2021) UniProt: the universal protein knowledgebase in 2021. Nucleic Acids Res 49:D480–D489. https://doi.org/10.1093/nar/gkaa1100
5. Benesh AE, Nambiar R, McConnell RE et al (2010) Differential localization and dynamics of class I myosins in the enterocyte microvillus. Mol Biol Cell 21:970–978. https://doi.org/10.1091/mbc.E09-07-0638
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