Abstract:
:Rett syndrome affects young girls. The molecular basis is mysterious. One tenable hypothesis can be that the programmed early infantile death of neuronal cells is reprogrammed. The bcl-2 gene on chromosome 22 has been shown to play a role in the apoptosis process. No sequence abnormalities were detected in the bcl-2 gene of 6 patients with Rett syndrome which could explain the pathophysiology of Rett syndrome.
journal_name
Neuropediatricsjournal_title
Neuropediatricsauthors
Anvret M,Zhang ZP,Hagberg Bdoi
10.1055/s-2008-1073047subject
Has Abstractpub_date
1994-12-01 00:00:00pages
323-4issue
6eissn
0174-304Xissn
1439-1899journal_volume
25pub_type
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