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Tytuł pozycji:

脑性瘫痪的遗传学研究进展. (Chinese)

Tytuł:
脑性瘫痪的遗传学研究进展. (Chinese)
Autorzy:
王芳芳
罗蓉
屈艺
母得志
Alternatywny tytuł:
Advances in genetic research of cerebral palsy. (English)
Źródło:
Chinese Journal of Contemporary Pediatrics; Sep2017, Vol. 19 Issue 9, p1022-1026, 5p
Abstract (English):
Cerebral palsy is a group of syndromes caused by non-progressive brain injury in the fetus or infant and can cause disabilities in childhood. Etiology of cerebral palsy has always been a hot topic for clinical scientists. More and more studies have shown that genetic factors are closely associated with the development of cerebral palsy. With the development and application of various molecular and biological techniques such as chromosome microarray analysis, genome-wide association study, and whole exome sequencing, new achievements have been made in the genetic research of cerebral palsy. Chromosome abnormalities, copy number variations, susceptibility genes, and single gene mutation associated with the development of cerebral palsy have been identified, which provides new opportunities for the research on the pathogenesis of cerebral palsy. This article reviews the advances in the genetic research on cerebral palsy in recent years. [ABSTRACT FROM AUTHOR]
Czasopismo naukowe
Copyright of Chinese Journal of Contemporary Pediatrics is the property of Xiangya Medical Periodical Press and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

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