HPRTSardinia: a new point mutation causing HPRT deficiency without Lesch–Nyhan disease-Reference-Cited by-同舟云学术

HPRTSardinia: a new point mutation causing HPRT deficiency without Lesch–Nyhan disease

Published:2006-01 Issue:1 Volume:1762 Page:29-33
ISSN:0925-4439
Container-title:Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
language:en
Short-container-title:Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease

Author:

Cossu Antonello,Orrù Sandro,Jacomelli Gabriella,Carcassi Carlo,Contu Licinio,Sestini Silvia,Corradi Maria Rita,Pompucci Giuseppe,Carcassi Aldo,Micheli Vanna

Publisher

Elsevier BV

Subject

Molecular Biology,Molecular Medicine

Reference22 articles.

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3. Diagnosis and treatment of the Lesch–Nyhan syndrome;Crawhall;Pediatr. Res.,1972

4. The biochemical basis of the behavioural disorder in the Lesch–Nyhan syndrome;Baumeister;Neurosci. Biobehav. Rev.,1985

5. A specific enzyme defect in gout associated with overproduction of uric acid;Kelley;Proc. Natl. Acad. Sci.,1967

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