Disorders of metal metabolism

Author:

Ferreira Carlos R.123,Gahl William A.3

Affiliation:

1. Division of Genetics and Metabolism, Children’s National Health System, Washington, DC, USA

2. Department of Pediatrics, George Washington University School of Medicine and Health Sciences, Washington, DC, USA

3. Section on Human Biochemical Genetics, Medical Genetics Branch, National Human Genome Research Institute, NIH, Bethesda, MD, USA

Publisher

IOS Press

Subject

General Medicine

Reference248 articles.

1. Culotta V.C. and Gitlin J.D. , Disorders of Copper Transport. In: Valle DL , Beaudet AL , Vogelstein B , Kinzler KW , Antonarakis SE , Ballabio A , et al., editors. The Online Metabolic and MolecularBases of Inherited Disease [Internet]. New York NY: The McGraw-Hill Comanies, Inc.; 2014 [cited 2015 Jul 27]. Available from: http://mhmedical.com/content.aspx?aid=1102891541

2. The elusive function of metallothioneins;Palmiter;Proc Natl Acad Sci U S A,1998

3. Progressive lenticular degeneration: A familial nervous disease associated with cirrhosis of the liver;Wilson;Brain,1912

4. Weiss K.H. , Wilson Disease. In: Pagon RA , Adam MP , Ardinger HH , Wallace SE , Amemiya A , Bean LJ , et al., editors. GeneReviews(®) [Internet]. Seattle (WA): University of Washington, Seattle; 1993 [cited 2015 Aug 6]. Available from: http://www.ncbi.nlm.nih.gov/books/NBK1512/

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