Mutation of KCNJ8 in a patient with Cantú syndrome with unique vascular abnormalities – Support for the role of K(ATP) channels in this condition-Reference-Cited by-同舟云学术

Mutation of KCNJ8 in a patient with Cantú syndrome with unique vascular abnormalities – Support for the role of K(ATP) channels in this condition

Published:2013-12 Issue:12 Volume:56 Page:678-682
ISSN:1769-7212
Container-title:European Journal of Medical Genetics
language:en
Short-container-title:European Journal of Medical Genetics

Author:

Brownstein Catherine A.,Towne Meghan C.,Luquette Lovelace J.,Harris David J.,Marinakis Nicholas S.,Meinecke Peter,Kutsche Kerstin,Campeau Philippe M.^ORCID,Yu Timothy W.,Margulies David M.,Agrawal Pankaj B.,Beggs Alan H.

Funder

National Institutes of Health

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics,General Medicine

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