Author:
Alazami AM,Schneider SA,Bonneau D,Pasquier L,Carecchio M,Kojovic M,Steindl K,De Kerdanet M,Nezarati MM,Bhatia KP,Degos B,Goh E,Alkuraya FS
Subject
Genetics(clinical),Genetics
Reference9 articles.
1. A syndrome of hypogonadism, alopecia, diabetes mellitus, mental retardation, deafness, and ECG abnormalities;Woodhouse;J Med Genet,1983
2. 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
3. Dystonia in the Woodhouse Sakati syndrome: A new family and literature review;Steindl;Mov Disord,2008
4. Steindl K Alazami AM Bhatia KP Wuerfel J Petersen D Klein C Mongiardo B Alkuraya FS Schneider SA. A novel C2orf37 mutation causes the first Italian cases of Woodhouse Sakati syndrome Clin Genet
5. Mutations in C2orf37, encoding a nucleolar protein, cause hypogonadism, alopecia, diabetes mellitus, mental retardation, and extrapyramidal syndrome;Alazami;Am J Hum Genet,2008
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