Recent developments in Menkes disease

Author:

Kodama H.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference31 articles.

1. Chelly J, Tümer Z, Tønnesen T et al (1993) Isolation of a candidate gene for Menkes disease that encodes a potential heavy metal binding protein.Nature Genetics 3: 14?19.

2. Danks DM (1989) Disorders of copper transport. In Scriver CR, Beaudet AL, Sly WS, Valle D, eds.The Metabolic Basis of Inherited Disease, 6th edn. New York: McGraw-Hill, 1411?1431.

3. Danks DM, Campbell PE, Steevens BJ, Mayne V, Cartwright E (1972) Menke's kinky hair syndrome: An inherited defect in copper absorption with widespread effects.Pediatrics 50: 188?120.

4. Fujii T, Okuno T, Ito M et al (1991) Non-Menkes-type copper deficiency with regression, lactic acidosis, and granulocytopenia.Neurology 41: 1263?1266.

5. Gerdes AM, Tønnesen T, Pergament E et al (1989) Variability in clinical expression of Menkes syndrome.Eur J Pediatr 148: 132?135.

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