| Literature DB >> 15986422 |
Galit Kleiner-Fisman1, Noel Y Calingasan, Mary Putt, June Chen, M Flint Beal, Anthony E Lang.
Abstract
Benign hereditary chorea (BHC) recently has been associated with mutations in TITF-1 gene, although a pathological study of an individual with BHC and a TITF-1 mutation revealed no significant gross or microscopic abnormalities using standard methods. Immunohistochemical staining of striatal tissue from a BHC-affected postmortem brain was performed using antibodies against neurotransmitters of interneurons whose tangential migration is mediated by TITF-1. There was a loss of most TITF-1-mediated striatal interneurons in the BHC specimen compared to four matched control brains. Copyright (c) 2005 Movement Disorder Society.Entities:
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Year: 2005 PMID: 15986422 DOI: 10.1002/mds.20577
Source DB: PubMed Journal: Mov Disord ISSN: 0885-3185 Impact factor: 10.338