sodium/bile acid cotransporter 7 isoform d [Mus musculus]

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A New SLC10A7 Homozygous Missense Mutation Responsible for a Milder Phenotype of Skeletal Dysplasia With Amelogenesis Imperfecta. [Front Genet. 2019]
A New SLC10A7 Homozygous Missense Mutation Responsible for a Milder Phenotype of Skeletal Dysplasia With Amelogenesis Imperfecta.
Laugel-Haushalter V, Bär S, Schaefer E, Stoetzel C, Geoffroy V, Alembik Y, Kharouf N, Huckert M, Hamm P, Hemmerlé J, et al. Front Genet. 2019; 10:504. Epub 2019 May 28.
SLC10A7 mutations cause a skeletal dysplasia with amelogenesis imperfecta mediated by GAG biosynthesis defects. [Nat Commun. 2018]
SLC10A7 mutations cause a skeletal dysplasia with amelogenesis imperfecta mediated by GAG biosynthesis defects.
Dubail J, Huber C, Chantepie S, Sonntag S, Tüysüz B, Mihci E, Gordon CT, Steichen-Gersdorf E, Amiel J, Nur B, et al. Nat Commun. 2018 Aug 6; 9(1):3087. Epub 2018 Aug 6.
Molecular and phylogenetic characterization of a novel putative membrane transporter (SLC10A7), conserved in vertebrates and bacteria. [Eur J Cell Biol. 2007]
Molecular and phylogenetic characterization of a novel putative membrane transporter (SLC10A7), conserved in vertebrates and bacteria.
Godoy JR, Fernandes C, Döring B, Beuerlein K, Petzinger E, Geyer J. Eur J Cell Biol. 2007 Aug; 86(8):445-60. Epub 2007 Jul 12.

RefSeq mRNA
See reference mRNA sequence for the Slc10a7 gene (NM_001282108.1).
RefSeq protein isoforms
See 10 reference sequence protein isoforms for the Slc10a7 gene.

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