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Identification of RNF13 as cause of recessively inherited ALS in a multi-case pedigree.
J Med Genet. 2022 Jul 25:jmedgenet-2022-108645. doi: 10.1136/jmg-2022-108645. Online ahead of print.
J Med Genet. 2022.
PMID: 35879052
HMSN-P caused by p.Pro285Leu mutation in TFG is not confined to patients with Far East ancestry.
Alavi A, Shamshiri H, Nafissi S, Khani M, Klotzle B, Fan JB, Steemers F, Elahi E.
Alavi A, et al.
Neurobiol Aging. 2015 Mar;36(3):1606.e1-7. doi: 10.1016/j.neurobiolaging.2014.11.021. Epub 2014 Dec 16.
Neurobiol Aging. 2015.
PMID: 25725944
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