small G protein signaling modulator 3 isoform 7 [Homo sapiens]

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Intellectual disability syndrome associated with a homozygous founder variant in SGSM3 in Ashkenazi Jews. [J Med Genet. 2024]
Intellectual disability syndrome associated with a homozygous founder variant in SGSM3 in Ashkenazi Jews.
Birnbaum R, Ezer S, Lotan NS, Eilat A, Sternlicht K, Benyamini L, Reish O, Falik-Zaccai T, Ben-Gad G, Rod R, et al. J Med Genet. 2024 Feb 21; 61(3):289-293. Epub 2024 Feb 21.
Evaluation of 4-bp insertion/deletion polymorphism within the 3'UTR of SGSM3 in bladder cancer using mismatch PCR-RFLP method: A preliminary report. [J Cell Biochem. 2018]
Evaluation of 4-bp insertion/deletion polymorphism within the 3'UTR of SGSM3 in bladder cancer using mismatch PCR-RFLP method: A preliminary report.
Hashemi M, Bahari G, Bizhani F, Danesh H, Sarhadi S, Ziaee SAM, Basiri A, Narouie B, Taheri M, Ghavami S. J Cell Biochem. 2018 Aug; 119(8):6566-6574. Epub 2018 Apr 25.
Association between an insertion/deletion polymorphism within 3'UTR of SGSM3 and risk of hepatocellular carcinoma. [Tumour Biol. 2014]
Association between an insertion/deletion polymorphism within 3'UTR of SGSM3 and risk of hepatocellular carcinoma.
Wang C, Zhao H, Zhao X, Wan J, Wang D, Bi W, Jiang X, Gao Y. Tumour Biol. 2014 Jan; 35(1):295-301. Epub 2013 Aug 6.

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