Browsing by Author "Per H."
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A family with mental retardation, epilepsy and cerebellar hypoplasia showing linkage to chromosome 20p11.21-q11.23
Bayrakli F.; Canpolat M.; Per H.; Gumus H.; Kumandas S.; Kartal U.; Balaban H. (2014)Background: Cerebellar hypoplasia (CH) is a rare malformation caused by various etiologies, usually manifesting clinically as nonprogressive cerebellar ataxia with or without mental retardation. The molecular pathogenesis ...