Fusion protein amino acids 1168-1237 of rat Slo2.2 (Slack); NP_068625
特徴および利点
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物理的形状
Solution in PBS, pH 7.4, 50% glycerol, and 0.09% sodium azide
免責事項
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Human molecular genetics, 26(11), 2042-2052 (2017-03-24)
De novo and inherited mutations of X-chromosome cell adhesion molecule protocadherin 19 (PCDH19) cause frequent, highly variable epilepsy, autism, cognitive decline and behavioural problems syndrome. Intriguingly, hemizygous null males are not affected while heterozygous females are, contradicting established X-chromosome inheritance.