ATP7A Gene Addition to the Choroid Plexus Results in Long-term Rescue of the Lethal Copper Transport Defect in a Menkes Disease Mouse Model

Author:

Donsante Anthony,Yi Ling,Zerfas Patricia M,Brinster Lauren R,Sullivan Patricia,Goldstein David S,Prohaska Joseph,Centeno Jose A,Rushing Elisabeth,Kaler Stephen G

Publisher

Elsevier BV

Subject

Drug Discovery,Pharmacology,Genetics,Molecular Biology,Molecular Medicine

Reference50 articles.

1. A sex-linked recessive disorder with retardation of growth, peculiar hair, and focal cerebral and cerebellar degeneration;Menkes;Pediatrics,1962

2. Isolation of a candidate gene for Menkes disease and evidence that it encodes a copper-transporting ATPase;Vulpe;Nat Genet,1993

3. Isolation of a candidate gene for Menkes disease that encodes a potential heavy metal binding protein;Chelly;Nat Genet,1993

4. Isolation of a partial candidate gene for Menkes disease by positional cloning;Mercer;Nat Genet,1993

5. ATP7A-related copper transport diseases-emerging concepts and future trends;Kaler;Nat Rev Neurol,2011

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