DCAF17

Publications

Alazami AM et al. Mutations in C2orf37, encoding a nucleolar protein, cause hypogonadism, alopecia, diabetes mellitus, mental retardation, and extrapyramidal syndrome.  Am J Hum Genet. 2008;83(6):684-691.  PMID:19026396.

Alazami AM et al.C2orf37 mutational spectrum in Woodhouse–Sakati syndrome patients. Clin Genet. 2010;78(6):585-590.  PMID:20507343.