Homo sapiens mutS homolog 4 (E. coli) (MSH4) gene, complete cds

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A novel homozygote nonsense variant of MSH4 leads to primary ovarian insufficiency and non-obstructive azoospermia. [Mol Biol Rep. 2024]
A novel homozygote nonsense variant of MSH4 leads to primary ovarian insufficiency and non-obstructive azoospermia.
Hashemi Sheikhshabani S, Ghafouri-Fard S, Hosseini E, Omrani MD. Mol Biol Rep. 2024 Jan 4; 51(1):68. Epub 2024 Jan 4.
Identification of compound heterozygous variants in MSH4 as a novel genetic cause of diminished ovarian reserve. [Reprod Biol Endocrinol. 2023]
Identification of compound heterozygous variants in MSH4 as a novel genetic cause of diminished ovarian reserve.
Wan Y, Hong Z, Ma B, He X, Ma L, Wang M, Zhang Y. Reprod Biol Endocrinol. 2023 Aug 24; 21(1):76. Epub 2023 Aug 24.
CFTR interactome mapping using the mammalian membrane two-hybrid high-throughput screening system. [Mol Syst Biol. 2022]
CFTR interactome mapping using the mammalian membrane two-hybrid high-throughput screening system.
Lim SH, Snider J, Birimberg-Schwartz L, Ip W, Serralha JC, Botelho HM, Lopes-Pacheco M, Pinto MC, Moutaoufik MT, Zilocchi M, et al. Mol Syst Biol. 2022 Feb; 18(2):e10629.

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Nucleotide