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C2orf37

WebNov 2, 2010 · C2orf37 mutational spectrum in Woodhouse–Sakati syndrome patients. Woodhouse–Sakati syndrome (WSS) is a rare autosomal recessive disorder that encompasses hypogonadism, deafness, alopecia, mental retardation, diabetes mellitus and progressive extrapyramidal defects. The syndrome is caused by mutation of the C2orf37 … Web首页; 代理品牌. 产品类型; 品牌介绍; 定制/代测; 欣博盛品牌. 产品类型; 奖学金活动; 代测服务; 客户评鉴; 文献引用; 新闻资讯

C2orf37 antibody (26033-1-AP) Proteintech - ptglab

WebDec 15, 2011 · Linkage in the family was established to the gene C2orf37, mapped on chromosome 2q22.3-2q35. DNA sequence analysis revealed a novel splice site mutation involving a homozygous G→A transition in the splice donor site of intron 3 (c.321+1G>A) of C2orf37. This study presents a first report of Woodhouse-Sakati syndrome identified in … 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 akb0048第一季免费观看全集 https://bexon-search.com

Anti-DCAF17 / C2orf37 Antibody Rabbit anti-Human Polyclonal …

WebNov 20, 2008 · Our data revealed a common founder mutation in C2orf37 as the cause of WSS in all the Saudi families we examined, including the ones originally described by Woodhouse and Sakati. Subsequent … http://www.neobioscience.com/prod_view.aspx?TypeId=409&Id=1338985&FId=t3:409:3 WebC2orf37 gene in the index patient and confirmed the diagnosis of WSS. Further analyses revealed that this mutation was also present in a homozygous state akb 歌詞 名言

A novel splice site mutation in gene C2orf37 underlying …

Category:C2orf37 antibody (26033-1-AP) Proteintech - ptglab

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C2orf37

A novel splice site mutation in gene C2orf37 underlying …

WebSep 30, 2011 · How to Cite this Article: Ben-Omran T, Ali R, Almureikhi M, Alameer S, Al-Saffar M, Walsh CA, Felie JM, Teebi A. 2011. Phenotypic heterogeneity in Woodhouse–Sakati syndrome: Two new families with a mutation in the C2orf37 gene. Am J Med Genet Part A 155: 2647–2653. 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.

C2orf37

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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 … WebZestimate® Home Value: $448,000. 3037 NW 92nd Ave, Coral Springs, FL is a multi family home that contains 1,500 sq ft and was built in 1989. It contains 4 bedrooms and 2 …

WebDec 1, 2010 · C2orf37 mutational spectrum in Woodhouse–Sakati syndrome patients. Woodhouse–Sakati syndrome (WSS) is a rare autosomal recessive disorder that encompasses hypogonadism, deafness, alopecia ... WebApr 1, 2015 · C2orf37 mutational spectrum in Woodhouse–Sakati syndrome patients. Woodhouse–Sakati syndrome (WSS) is a rare autosomal recessive disorder that encompasses hypogonadism, deafness, alopecia ...

WebDec 15, 2011 · Woodhouse-Sakati Syndrome (WSS) is a rare autosomal recessive multisystemic disorder that is marked by hypogonadism, alopecia, intellectual disability, … Web本发明提供了一种具有降低的脱靶效应的基因编辑系统，包括(a)包含编码核酸酶的核酸序列的载体，其中编码核酸酶的核酸在其序列内包含调控核酸序列，该调控核酸序列具有定义第一内含子和第二内含子的第一组剪接元件和第二组剪接元件，其中第一内含子和第二内含子在编码包含符合读框的终止 ...

WebMar 21, 2024 · A novel C2orf37 mutation causes the first Italian cases of Woodhouse Sakati syndrome C2orf37 mutational spectrum in Woodhouse-Sakati syndrome patients …

WebSep 9, 2013 · Direct sequencing of the C2orf37 gene revealed that the c.436delC (p.Ala147Hisfs*9) mutation was present in a homozygous state in all affected siblings and in a heterozygous state in the parents and a healthy sister. Nine C2orf37 mutations causing WSS have been identified. This family shared the mutation reported earlier in Saudi … taupadak sexualidadWeb"C2orf37 antibodies" comparison At Proteintech, we pride ourselves on our antibody quality, customer service and transparency. As such, we are comparing our antibodies with other vendors, enabling easy identification … taupadak hip hopProteintech Anti-C2orf37 Polyclonal, Catalog # 26033-1-AP. Tested in Western Blot (WB) and Immunohistochemistry (Paraffin) (IHC (P)) applications. This antibody reacts with Human, Mouse samples. Supplied as 150 µL purified antibody (0.3 mg/mL). ak不動産 日田akb149 1 恋愛総選挙 攻略WebThe DCAF17 gene provides instructions for making a protein whose function is unknown. The gene is active (expressed) in several organs and tissues in the body, including the … akb 歌唱力決定戦WebSupplier Page from Proteintech Group Inc for C2orf37 antibody. Product Specs; Company Info; Reviews; Product Specs; Item C2orf37 antibody; Company Proteintech Group Inc; Price Pricing Info Supplier Page View Company Product Page; Catalog Number 26033-1-AP; Quantity 20ul, 150ul; Applications WB, IHC, ELISA; taupadak pamplonaWeb开馆时间：周一至周日7:00-22:30 周五 7:00-12:00; 我的图书馆 ak15少女前线萌娘百科