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t/gene-kcnj2

KCNJ2 gene

Discuss publications and research concerning the KCNJ2 gene.

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Related literature

Chromosomal Rearrangements Identified in Three Additional Patients With Generalized Congenital Hypertrichosis With Gingival Hyperplasia Involving the 17q24.2-q24.3 Locus.
KCNJ2
Gene and allele-specific expression during electric organ ontogeny in African weakly electric fish (Campylomormyrus).
KCNJ2
Clinical features and advances in the genetics of periodic paralysis.
KCNJ2
When the U Wave Tells the Story: Andersen-Tawil Syndrome Unmasked.
KCNJ2
Phenotypic Variability of Andersen-Tawil Syndrome Due to Allelic Mutation c.652C>T in the KCNJ2 Gene-A New Family Case Report.
KCNJ2
Gene and Allele-Specific Expression Underlying the Electric Signal Divergence in African Weakly Electric Fish.
KCNJ2
Association of KCNJ2 Genetic Variants with Susceptibility to Thyrotoxic Periodic Paralysis in Patients with Graves' Disease.
KCNJ2
Coexistence of Andersen-Tawil Syndrome with Polymorphisms in hERG1 Gene (K897T) and SCN5A Gene (H558R) in One Family.
KCNJ2
Case report: A Chinese child with Andersen-Tawil syndrome due to a de novo KCNJ2 mutation.
KCNJ2
Andersen-Tawil syndrome with early fixed myopathy.
KCNJ2

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