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A model of behavioral treatments for self-mutilation behavior in Lesch-Nyhan syndrome
Lesch-Nyhan syndrome is a rare genetic disorder, caused by a mutation in the gene coding for the enzyme hypoxanthine-guanine phosphoribosyltransferase (HPRT), which is characterized by hyperuricemia and its associated symptoms along with motor disorders and compulsive self-mutilation. We show that t...
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| Main Authors: | , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
2008
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2408668/ https://ncbi.nlm.nih.gov/pubmed/18287946 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/WNR.0b013e3282f5f76f |
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