Eur J Med Genet
http://www.ncbi.nlm.nih.gov/pubmed/24176758
56(12):678-82
https://connects.catalyst.harvard.edu/Profiles/profile/67604379
Mutation of KCNJ8 in a patient with Cantú syndrome with unique vascular abnormalities - support for the role of K(ATP) channels in this condition.
Eur J Med Genet
http://www.ncbi.nlm.nih.gov/pubmed/24176758
56(12):678-82
https://connects.catalyst.harvard.edu/Profiles/profile/67604379