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XB--6042120
Papers associated with cacna1h (and Disease Ontology)
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Functional variants in HCN4 and CACNA1H may contribute to genetic generalized epilepsy., Becker F, Reid CA, Hallmann K, Tae HS, Phillips AM, Teodorescu G, Weber YG, Kleefuss-Lie A, Elger C, Perez-Reyes E, Petrou S, Kunz WS, Lerche H, Maljevic S., Epilepsia Open. August 5, 2017; 2 (3): 334-342.  |
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A revised mechanism of action of hyperaldosteronism-linked mutations in cytosolic domains of GIRK4 (KCNJ5)., Shalomov B, Handklo-Jamal R, Reddy HP, Theodor N, Bera AK, Dascal N., J Physiol. March 1, 2022; 600 (6): 1419-1437. |
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