amyotrophic lateral sclerosis 2 (juvenile) homolog (human), isoform CR - Protein

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Absence of alsin function leads to corticospinal motor neuron vulnerability via novel disease mechanisms. [Hum Mol Genet. 2016]
Absence of alsin function leads to corticospinal motor neuron vulnerability via novel disease mechanisms.
Gautam M, Jara JH, Sekerkova G, Yasvoina MV, Martina M, Özdinler PH. Hum Mol Genet. 2016 Mar 15; 25(6):1074-87. Epub 2016 Jan 10.
Genetic background and gender effects on gross phenotypes in congenic lines of ALS2/alsin-deficient mice. [Neurosci Res. 2010]
Genetic background and gender effects on gross phenotypes in congenic lines of ALS2/alsin-deficient mice.
Hadano S, Yoshii Y, Otomo A, Kunita R, Suzuki-Utsunomiya K, Pan L, Kakuta S, Iwasaki Y, Iwakura Y, Ikeda JE. Neurosci Res. 2010 Oct; 68(2):131-6. Epub 2010 Jun 14.
Regulation of endosomal motility and degradation by amyotrophic lateral sclerosis 2/alsin. [Mol Brain. 2009]
Regulation of endosomal motility and degradation by amyotrophic lateral sclerosis 2/alsin.
Lai C, Xie C, Shim H, Chandran J, Howell BW, Cai H. Mol Brain. 2009 Jul 24; 2:23. Epub 2009 Jul 24.

RefSeq protein isoforms
See 3 reference sequence protein isoforms for the Als2 gene.

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