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美国心、肺、血研究所(NHLBI)和少见病办公室(ORD)于2006年9月14~15日在Bethesde联合召开了专题研讨会议,目的在于向NHLBI及ORD提出建议,需考虑以新的研究方向提高下列情况的识别和治疗:①罕见的遗传性钠通道病;②钾通道突变引起的罕见遗传性心律失常;③其他致心律失常机制造成
NHLBI and ORD co-hosted a panel discussion in Bethesde on September 14-15, 2006 with the objective of making recommendations to the NHLBI and the ORD, taking into account the new Research direction to improve the identification and treatment of the following conditions: ① rare hereditary sodium channel disease; ② potassium channel mutations caused by rare hereditary arrhythmia; ③ caused by other induced arrhythmia mechanism