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PubMed (cited) for id: 617460
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A missense mutation in HK1 leads to autosomal dominant retinitis pigmentosa.
Invest Ophthalmol Vis Sci. 2014 Oct 14;55(11):7159-64. doi: 10.1167/iovs.14-15520.
Invest Ophthalmol Vis Sci. 2014.
PMID: 25316723
Free PMC article.
A dominant mutation in hexokinase 1 (HK1) causes retinitis pigmentosa.
Sullivan LS, Koboldt DC, Bowne SJ, Lang S, Blanton SH, Cadena E, Avery CE, Lewis RA, Webb-Jones K, Wheaton DH, Birch DG, Coussa R, Ren H, Lopez I, Chakarova C, Koenekoop RK, Garcia CA, Fulton RS, Wilson RK, Weinstock GM, Daiger SP.
Sullivan LS, et al.
Invest Ophthalmol Vis Sci. 2014 Sep 4;55(11):7147-58. doi: 10.1167/iovs.14-15419.
Invest Ophthalmol Vis Sci. 2014.
PMID: 25190649
Free PMC article.
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