Human Genome Epidemiology Literature Finder
Rare Diseases
Records 1 - 1 (of 1 Records) |
Query Trace: Cerebellar Ataxia And Hypogonadotropic Hypogonadism[original query] |
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A novel mutation in RNF216 gene in a Turkish case with Gordon Holmes syndrome. BMC medical genomics 2023 5 16 (1): 98. Nazl? Durmaz Çelik, Ebru Erzurumluo?lu, Serkan Özben, U?ur Toprak, Göknur Yorulmaz, Sevilhan Artan, Serhat Özk |
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