In utero copper treatment for Menkes disease associated with a severe ATP7A mutation

Authors

Marie Reine Haddad, National Institutes of Health, Bethesda, MD
Charles Macri, George Washington UniversityFollow
Courtney S. Holmes, National Institutes of Health, Bethesda, MD
David S. Goldstein, National Institutes of Health, Bethesda, MD
Beryl E. Jacobson, BC Children's Hospital, Vancouver, BC, Canada
Jose A. Centeno, The Joint Pathology Center, Silver Spring, MD
Edwina J. Popek, Baylor College of Medicine
Willam A. Gahl, National Institutes of Health
Stephen G. Kaler, National Institutes of Health, Bethesda, MD

Document Type

Journal Article

Publication Date

9-2012

Journal

Molecular Genetics and Metabolism

Volume

Volume 107, Issue 1-2

Inclusive Pages

222-228

Keywords

Adenosine Triphosphatases--genetics; Cation Transport Proteins--genetics; Fetus--drug effects; Histidine--analogs & derivatives; Menkes Kinky Hair Syndrome--drug therapy; Menkes Kinky Hair Syndrome--genetics; Mutation; Organometallic Compounds--therapeutic use

Comments

This is a PubMed Central article. Click on link for full-text access.

APA Citation

Haddad, M. R., Macri, C. J., Holmes, C. S., Goldstein, D. S., Jacobson, B. E., Centeno, J. A., Popek, E.J., Gahl, W.A. Kaler, S. G. (2012). In utero copper treatment for menkes disease associated with a severe ATP7A mutation. Molecular Genetics and Metabolism, 107(1-2), 222-228.

Peer Reviewed

1

Open Access

1