proton channel OTOP2 [Mus musculus]

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Biallelic mutations in the ferredoxin reductase gene cause novel mitochondriopathy with optic atrophy. [Hum Mol Genet. 2017]
Biallelic mutations in the ferredoxin reductase gene cause novel mitochondriopathy with optic atrophy.
Peng Y, Shinde DN, Valencia CA, Mo JS, Rosenfeld J, Truitt Cho M, Chamberlin A, Li Z, Liu J, Gui B, et al. Hum Mol Genet. 2017 Dec 15; 26(24):4937-4950.
Mutations in a new scaffold protein Sans cause deafness in Jackson shaker mice. [Hum Mol Genet. 2003]
Mutations in a new scaffold protein Sans cause deafness in Jackson shaker mice.
Kikkawa Y, Shitara H, Wakana S, Kohara Y, Takada T, Okamoto M, Taya C, Kamiya K, Yoshikawa Y, Tokano H, et al. Hum Mol Genet. 2003 Mar 1; 12(5):453-61.
An evolutionarily conserved gene family encodes proton-selective ion channels. [Science. 2018]
An evolutionarily conserved gene family encodes proton-selective ion channels.
Tu YH, Cooper AJ, Teng B, Chang RB, Artiga DJ, Turner HN, Mulhall EM, Ye W, Smith AD, Liman ER. Science. 2018 Mar 2; 359(6379):1047-1050. Epub 2018 Jan 25.

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Protein