APC Membran-Rekrutierungsprotein 1

Jenkins ZA et al. (2009) Germline mutations in WTX cause a sclerosing skeletal dysplasia but do not predispose to tumorigenesis.

Perdu B et al. (2010) Osteopathia striata with cranial sclerosis owing to WTX gene defect.

Perdu B et al. (2011) Two novel WTX mutations underscore the unpredictability of male survival in osteopathia striata with cranial sclerosis.

Holman SK et al. (2011) The male phenotype in osteopathia striata congenita with cranial sclerosis.

König R et al. (1996) Osteopathia striata with cranial sclerosis: variable expressivity in a four generation pedigree.

Keymolen K et al. (1997) How to counsel in osteopathia striata with cranial sclerosis.

Savarirayan R et al. (1997) Osteopathia striata with cranial sclerosis: highly variable phenotypic expression within a family.

Rivera MN et al. (2007) An X chromosome gene, WTX, is commonly inactivated in Wilms tumor.

Ota T et al. (2004) Complete sequencing and characterization of 21,243 full-length human cDNAs.

Kimura K et al. (2006) Diversification of transcriptional modulation: large-scale identification and characterization of putative alternative promoters of human genes.

Major MB et al. (2007) Wilms tumor suppressor WTX negatively regulates WNT/beta-catenin signaling.

Grohmann A et al. (2007) AMER1 regulates the distribution of the tumor suppressor APC between microtubules and the plasma membrane.

NCBI article

OMIM.ORG article

Orphanet article