zinc finger protein 41 isoform d [Homo sapiens]

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Mutations in the ZNF41 gene are associated with cognitive deficits: identification of a new candidate for X-linked mental retardation. [Am J Hum Genet. 2003]
Mutations in the ZNF41 gene are associated with cognitive deficits: identification of a new candidate for X-linked mental retardation.
Shoichet SA, Hoffmann K, Menzel C, Trautmann U, Moser B, Hoeltzenbein M, Echenne B, Partington M, Van Bokhoven H, Moraine C, et al. Am J Hum Genet. 2003 Dec; 73(6):1341-54. Epub 2003 Nov 18.
Isolation and expression analysis of a human zinc finger gene (ZNF41) located on the short arm of the X chromosome. [Genomics. 1991]
Isolation and expression analysis of a human zinc finger gene (ZNF41) located on the short arm of the X chromosome.
Franzè A, Archidiacono N, Rocchi M, Marino M, Grimaldi G. Genomics. 1991 Apr; 9(4):728-36.
Coding region intron/exon organization, alternative splicing, and X-chromosome inactivation of the KRAB/FPB-domain-containing human zinc finger gene ZNF41. [Cytogenet Cell Genet. 1999]
Coding region intron/exon organization, alternative splicing, and X-chromosome inactivation of the KRAB/FPB-domain-containing human zinc finger gene ZNF41.
Rosati M, Franzé A, Matarazzo MR, Grimaldi G. Cytogenet Cell Genet. 1999; 85(3-4):291-6.

RefSeq genomic sequence
See the genomic reference sequence for the ZNF41 gene (NG_008238.1).
RefSeq protein isoforms
See 68 reference sequence protein isoforms for the ZNF41 gene.

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