A syndrome of epilepsy, dementia, and amelogenesis imperfecta: genetic and clinical features.
AUTOR(ES)
Christodoulou, J
RESUMO
A family is described with six members affected by a syndrome of epilepsy, dementia, and amelogenesis imperfecta (Kohlschütter's syndrome). An autosomal recessive pattern of inheritance is established for this disorder.
ACESSO AO ARTIGO
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=1051610Documentos Relacionados
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