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Content and distribution of haptoglobin phenotypes in children with cerebral palsy complicated by symptomatic epilepsy
Abstract
The genetic aspects of the development of various diseases are attracting close attention of researchers. Discussions are underway about the genetic predisposition of an individual to a particular pathology. First of all, this is relevant in the development of hereditary neurological diseases, many of which are manifested in early childhood.Other Versions
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