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    유전성 골격근 이온통로병 원인 예측방법을 수행하기 위한 컴퓨터 프로그램이 수록된 컴퓨터로 읽을 수 있는 기록매체 및 이를 실행시키는 장치
    2.
    发明公开
    유전성 골격근 이온통로병 원인 예측방법을 수행하기 위한 컴퓨터 프로그램이 수록된 컴퓨터로 읽을 수 있는 기록매체 및 이를 실행시키는 장치 有权
    计算机可读介质记录计算机程序来执行用于预测骨骼肌肉通道病变的原因的方法

    公开(公告)号：KR1020140007540A

    公开(公告)日：2014-01-20

    申请号：KR1020120074485

    申请日：2012-07-09

    Applicant: 전남대학교산학협력단

    Inventor： 김명규 ,  나인섭 ,  박상철

    IPC: G06F19/00 ,  G06F19/10

    CPC classification number: G06F19/18

    Abstract: Provided are a computer readable recording medium with a computer program and an executing apparatus thereof. The computer program of the recording medium quickly and accurately estimates a gene which causes a hereditary skeletal muscle channelopathy by performing a method for estimating the cause of the hereditary skeletal muscle channelopathy to determine the gene which causes the hereditary skeletal muscle channelopathy using information about episodic paralysis and myotonia. Thereby, a user quickly grasps the cause of the hereditary skeletal muscle channelopathy with low costs by testing a part of various genes which cause diseases. [Reference numerals] (AA) Start; (BB) End; (S110) Select at least one among episodic paralysis and myotonia; (S120) Input first symptom information corresponding to the episodic paralysis if the episodic paralysis is selected; (S130) Input second symptom information corresponding to the myotonia if the myotonia is selected; (S140) Determine the gene which causes the hereditary skeletal muscle channelopathy using the first and second symptom information; (S150) Display the gene which causes the hereditary skeletal muscle channelopathy on a screen

    Abstract translation: 提供一种具有计算机程序的计算机可读记录介质及其执行装置。 记录介质的计算机程序通过执行用于估计遗传性骨骼肌通道病变的原因的方法来快速准确地估计引起遗传性骨骼肌通道病变的基因，以使用关于发作性麻痹的信息来确定导致遗传性骨骼肌细胞通道病变的基因 和肌强直。 因此，通过测试造成疾病的各种基因的一部分，用户能够以低成本快速掌握遗传性骨骼肌通道病变的原因。 （附图标记）（AA）开始; （BB）结束; （S110）选择情节性麻痹和肌强直中的至少一种; （S120）如果选择了情节性麻痹，输入对应于情景性麻痹的第一症状信息; （S130）如果选择了肌强直，输入对应于肌强直的第二症状信息; （S140）使用第一和第二症状信息确定导致遗传性骨骼肌通道病变的基因; （S150）在屏幕上显示导致遗传性骨骼肌通道病变的基因

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