Homo sapiens solute carrier family 3 (cystine, dibasic and neutral ami - Nucleotide

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Novel compound heterozygous pathogenic variants in the SLC3A1 gene in a Chinese family with cystinuria. [BMC Med Genomics. 2023]
Novel compound heterozygous pathogenic variants in the SLC3A1 gene in a Chinese family with cystinuria.
Liu D, Zhao Y, Xue X, Hou X, Xu H, Zhao X, Tian Y, Tang W, Guo J, Xu C. BMC Med Genomics. 2023 Dec 19; 16(1):333. Epub 2023 Dec 19.
Population genetics analysis of SLC3A1 and SLC7A9 revealed the etiology of cystine stone may be more than what our current genetic knowledge can explain. [Urolithiasis. 2023]
Population genetics analysis of SLC3A1 and SLC7A9 revealed the etiology of cystine stone may be more than what our current genetic knowledge can explain.
Wu CW, Badreddine J, Chang J, Huang YM, Kim FJ, Wild T, Tsai AC, Meeks N, Donalisio Da Silva R, Molina WR, et al. Urolithiasis. 2023 Aug 10; 51(1):101. Epub 2023 Aug 10.
Interpretation of SLC3A1 and SLC7A9 variants in cystinuria patients: The significance of the PM3 criterion and protein stability. [Urolithiasis. 2023]
Interpretation of SLC3A1 and SLC7A9 variants in cystinuria patients: The significance of the PM3 criterion and protein stability.
Lee B, Lee SY, Han DH, Park HD. Urolithiasis. 2023 Jul 13; 51(1):94. Epub 2023 Jul 13.

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Homo sapiens solute carrier family 3 (cystine, dibasic and neutral amino acid tr...
Homo sapiens solute carrier family 3 (cystine, dibasic and neutral amino acid transporters, activator of cystine, dibasic and neutral amino acid transport), member 1, mRNA (cDNA clone MGC:120661 IMAGE:7939471), complete cds
gi|62739895|gb|BC093626.1|

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Nucleotide