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3-Hydroxy-3-methylglutaryl-CoA lyase deficiency in a boy with VATER association

M al-Essa¹, M Rashed, P T Ozand

¹Department of Pediatrics, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.

Journal of Inherited Metabolic Disease

|August 13, 1998

Abstract

No abstract available in PubMed .

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