PIP2 binding residues of Kir2.1 are common targets of mutations causing Andersen syndrome

Authors

M. R. Donaldson
J. L. Jensen
M. Tristani-Firouzi
R. Tawil
S. Bendahhou

Document Type

Journal Article

Publication Date

2003

Journal

Neurology

Volume

60

Issue

11

Inclusive Pages

1811-1816

APA Citation

Donaldson, M., Jensen, J., Tristani-Firouzi, M., Tawil, R., & Bendahhou, S. (2003). PIP2 binding residues of Kir2.1 are common targets of mutations causing Andersen syndrome. Neurology, 60 (11). Retrieved from https://hsrc.himmelfarb.gwu.edu/smhs_peds_facpubs/3962