Congenital absence of norepinephrine due to...

Neurology 2019 / 12

Congenital absence of norepinephrine due to CYB561 mutations

Shibao, Cyndya A., Garland, Emily M., Black, Bonnie K., Mathias, Christopher J., Grant, Maria B., Root, Allen W., Robertson, David, Biaggioni, Italo
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Language:
english
Journal:
Neurology
DOI:
10.1212/WNL.0000000000008734
Date:
December, 2019
File:
PDF, 241 KB
english, 2019
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