| Literature DB >> 2292045 |
H A Jinnah1, F H Gage, T Friedmann.
Abstract
In humans, deficiency of the enzyme hypoxanthine-guanine phosphoribosyltransferase (HPRT) is associated with a disorder known as Lesch-Nyhan syndrome which includes severe neurobehavioral abnormalities. Several animal models which have been developed to examine the neurobiologic substrates of this disorder have suggested a role for abnormal function in purine/dopamine neurotransmission, but the relationship between HPRT-deficiency and these abnormalities remains unknown. Recently, HPRT-deficient mice have been produced which appear to have similar, though more subtle changes in brain dopamine function. These mice will be useful in elucidating the relationship between HPRT-deficiency and the neurological deficits observed in patients with this disorder.Entities:
Mesh:
Year: 1990 PMID: 2292045 DOI: 10.1016/0361-9230(90)90239-v
Source DB: PubMed Journal: Brain Res Bull ISSN: 0361-9230 Impact factor: 4.077