hCG15400, isoform CRA_b [Homo sapiens]

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Systematic analysis of X-inactivation in 19XLMR families: extremely skewed profiles in carriers in three families. [Eur J Hum Genet. 2000]
Systematic analysis of X-inactivation in 19XLMR families: extremely skewed profiles in carriers in three families.
Raynaud M, Moizard MP, Dessay B, Briault S, Toutain A, Gendrot C, Ronce N, Moraine C. Eur J Hum Genet. 2000 Apr; 8(4):253-8.
Intellectual disability associated with retinal dystrophy in the Xp11.3 deletion syndrome: ZNF674 on trial. Guilty or innocent? [Eur J Hum Genet. 2012]
Intellectual disability associated with retinal dystrophy in the Xp11.3 deletion syndrome: ZNF674 on trial. Guilty or innocent?
Delphin N, Hanein S, Taie LF, Zanlonghi X, Bonneau D, Moisan JP, Boyle C, Nitschke P, Pruvost S, Bonnefont JP, et al. Eur J Hum Genet. 2012 Mar; 20(3):352-6. Epub 2011 Nov 30.
ZNF674: a new kruppel-associated box-containing zinc-finger gene involved in nonsyndromic X-linked mental retardation. [Am J Hum Genet. 2006]
ZNF674: a new kruppel-associated box-containing zinc-finger gene involved in nonsyndromic X-linked mental retardation.
Lugtenberg D, Yntema HG, Banning MJ, Oudakker AR, Firth HV, Willatt L, Raynaud M, Kleefstra T, Fryns JP, Ropers HH, et al. Am J Hum Genet. 2006 Feb; 78(2):265-78. Epub 2005 Dec 29.

RefSeq genomic sequence
See the genomic reference sequence for the ZNF674 gene (NG_023376.2).
RefSeq protein isoforms
See 5 reference sequence protein isoforms for the ZNF674 gene.

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