CONGENITAL DOPAMINE BETA-HYDROXYLASE DEFICIENCY

Author:

Superti-Furga Andrea,Royce PeterM.,Steinmann Beat,Man In't Veld A.J.,Boomsma F.,Schalekamp M.A.D.H.

Publisher

Elsevier BV

Subject

General Medicine

Reference15 articles.

1. Mutations affecting trace elements in humans and animals;Danks;Adv Hum Genet,1983

2. Copper metabolism in Menkes' disease;Horn,1984

3. Catecholamine biosynthesis and the activity of a number of copper dependent enzymes in the copper deficient mottled mouse mutants;Hunt;Comp Biochem Physiol,1977

4. Skeletal dysplasia, occipital horns, diarrhea and obstructive uropathya new hereditary syndrome;Lazoff;Birth Defects Orig Art Ser,1975

5. Abnormal copper metabolism and deficient lysyl oxidase activity in a heritable connective tissue disorder;Kuivaniemi;J Clin Invest,1982

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