Title : hKCNN3 which maps to chromosome 1q21 is not the causative gene in periodic catatonia, a familial subtype of schizophrenia.

Pub. Date : 2000

PMID : 11009068






2 Functional Relationships(s)
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Compound Name
Protein Name
Organism
1 The human calcium-activated potassium channel gene (hKCNN3, hSKCa3) contains two tandemly arranged, multiallelic CAG repeats located in exon 1 which result in short to moderate polyglutamine stretches of unknown functional significance. polyglutamine potassium calcium-activated channel subfamily N member 3 Homo sapiens
2 The human calcium-activated potassium channel gene (hKCNN3, hSKCa3) contains two tandemly arranged, multiallelic CAG repeats located in exon 1 which result in short to moderate polyglutamine stretches of unknown functional significance. polyglutamine potassium calcium-activated channel subfamily N member 3 Homo sapiens