Homo sapiens leucine rich repeat containing 66 (LRRC66), RefSeqGene on - Nucleotide

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Identification of a shared, common haplotype segregating with an SGCB c.544 T > G mutation in Indian patients affected with sarcoglycanopathy. [Sci Rep. 2023]
Identification of a shared, common haplotype segregating with an SGCB c.544 T > G mutation in Indian patients affected with sarcoglycanopathy.
Sanga S, Chakraborty S, Bardhan M, Polavarapu K, Kumar VP, Bhattacharya C, Nashi S, Vengalil S, Geetha TS, Ramprasad V, et al. Sci Rep. 2023 Sep 12; 13(1):15095. Epub 2023 Sep 12.
Comprehensive functional characterization of SGCB coding variants predicts pathogenicity in limb-girdle muscular dystrophy type R4/2E. [J Clin Invest. 2023]
Comprehensive functional characterization of SGCB coding variants predicts pathogenicity in limb-girdle muscular dystrophy type R4/2E.
Li C, Wilborn J, Pittman S, Daw J, Alonso-Pérez J, Díaz-Manera J, Weihl CC, Haller G. J Clin Invest. 2023 Jun 15; 133(12). Epub 2023 Jun 15.
Polymorphisms in the HSF2, LRRC6, MEIG1 and PTIP genes correlate with sperm motility in idiopathic infertility. [Andrologia. 2022]
Polymorphisms in the HSF2, LRRC6, MEIG1 and PTIP genes correlate with sperm motility in idiopathic infertility.
Gupta N, Sarkar S, Mehta P, Sankhwar SN, Rajender S. Andrologia. 2022 Oct; 54(9):e14517. Epub 2022 Jun 29.

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Nucleotide