WebDescription. C2orf37 antibody LS-C186957 is an unconjugated rabbit polyclonal antibody to human C2orf37 (DCAF17) (aa68-117). Validated for WB. WebDec 15, 2011 · Woodhouse–Sakati Syndrome (WSS) is a rare autosomal recessive multisystemic disorder that is marked by hypogonadism, alopecia, intellectual disability, deafness, diabetes mellitus and progressive extrapyramidal defects.Mutations in the gene C2orf37 are the cause of Woodhouse–Sakati syndrome. In the present study, a four …
Mutations in C2orf37, Encoding a Nucleolar Protein
WebView detailed information about property W10402 E 7th St, Black River Falls, WI 54615 including listing details, property photos, school and neighborhood data, and much more. WebC2orf37 antibody LS-C186957 is an unconjugated rabbit polyclonal antibody to human C2orf37 (DCAF17) (aa68-117). Validated for WB. Products. Research Areas. COVID-19. Resources. Contact Us. Distributors Login. Quick Order. Cart . Login. Registration enables users to use special features of this website, such as past combi beko b1rcne364w
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WebC7237 2.92F to 2.4F Adapter Centric RF. 800-399-6891. Login or Sign Up. 1130 Junction Dr. Suite 121 Allen, TX 75013 800-399-6891 [email protected]. 0. About Centric RF. … WebNovel compound heterozygous frameshift mutations of C2orf37 in a familial Indian case of Woodhouse-Sakati syndrome J Genet. 2015 Sep;94(3):489-92. doi: 10.1007/s12041-015-0544-7. Authors Mansoor C Abdulla 1 , Anas M Alazami, Jemshad Alungal, Jassim M Koya, Mohthash Musambil. Affiliation 1 Department of ... WebDec 1, 2008 · C2orf37 mutations were reported to be responsible for WSS in 2008 [5]. Nuclear C2orf37 overexpression was determined, compatibly with the disease … drug discovery scientist