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Mutation screening of the KCNN3 gene reveals a rare frameshift mutation.
Bowen T, Williams N, Norton N, Spurlock G, Wittekindt OH, Morris-Rosendahl DJ, Williams H, Brzustowicz L, Hoogendoorn B, Zammit S, Jones G, Sanders RD, Jones LA, McCarthy G, Jones S, Bassett A, Cardno AG, Owen MJ, O'Donovan MC. Bowen T, et al. Mol Psychiatry. 2001 May;6(3):259-60. doi: 10.1038/sj.mp.4000128. Mol Psychiatry. 2001. PMID: 11326292 No abstract available.
The human small conductance calcium-regulated potassium channel gene (hSKCa3) contains two CAG repeats in exon 1, is on chromosome 1q21.3, and shows a possible association with schizophrenia.
Wittekindt O, Jauch A, Burgert E, Schärer L, Holtgreve-Grez H, Yvert G, Imbert G, Zimmer J, Hoehe MR, Macher JP, Chiaroni P, van Calker D, Crocq MA, Morris-Rosendahl DJ. Wittekindt O, et al. Neurogenetics. 1998 Aug;1(4):259-65. doi: 10.1007/s100480050038. Neurogenetics. 1998. PMID: 10732800 Clinical Trial.
83 results