Mevalonate kinase deficiency in a dizygotic twin with mild mevalonic aciduria

Authors: Gibson K.M.^{1, 2}; Hoffmann G.F.³; Sweetman L.⁴; Buckingham B.⁵

Source: Journal of Inherited Metabolic Disease, Volume 20, Number 3, July 1997 , pp. 391-394(4)

Publisher: Springer

Abstract:

Language: English

Document Type: Short communication

Affiliations: 1: Institute of Metabolic Disease, Baylor Research Institute and Baylor University Medical Center, Dallas, Texas, USA 2: Department of Neurology, University of Texas Southwestern Medical Center, Dallas, Texas, USA 3: Department of Neuropediatrics and Metabolic Diseases, University Children's Hospital, Philipps University, Marburg, Germany 4: Department of Pediatrics, Division of Biochemical Genetics, Children's Hospital of Los Angeles and the University of Southern California School of Medicine, Los Angeles, California, USA 5: Department of Endocrinology and Metabolism, Children's Hospital of Orange County, Irvine, California, USA

Publication date: 1997-07-01

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• In this Subject: Internal Medicine
• By this author: Gibson K.M. ;  Hoffmann G.F. ;  Sweetman L. ;  Buckingham B.

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