Author:
Habib Rabia,Basit Sulman,Khan Saadullah,Khan Muhammad Nasim,Ahmad Wasim
Subject
Genetics,General Medicine
Reference20 articles.
1. Mutations in C2orf37, encoding a nucleolar protein, cause hypogonadism, alopecia, diabetes mellitus, mental retardation, and extrapyramidal syndrome;Alazami;Am. J. Hum. Genet.,2008
2. C2orf37 mutational spectrum in Woodhouse–Sakati syndrome patients;Alazami;Clin. Genet.,2010
3. Autosomal-recessive syndrome with alopecia, hypogonadism, progressive extra-pyramidal disorder, white matter disease, sensory neural deafness, diabetes mellitus, and low IGF1;Al-Semari;Am. J. Med. Genet. A,2007
4. Woodhouse Sakati syndrome associated with bilateral keratoconus;Al-Swailem;Br. J. Ophthalmol.,2006
5. The multifunctional nucleolus;Boisvert;Nat. Rev. Mol. Cell Biol.,2007
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