基本信息:
- 专利标题： 유전성 골격근 이온통로병 원인 예측방법을 수행하기 위한 컴퓨터 프로그램이 수록된 컴퓨터로 읽을 수 있는 기록매체 및 이를 실행시키는 장치
- 专利标题（英）：Computer readable medium recorded computer program to perform method for estimating reason for Hereditary Skeletal Muscle Channelopathy
- 专利标题（中）：计算机可读介质记录计算机程序以执行估计遗传性骨骼肌肉通道病变原因的方法
- 申请号：KR1020120074485 申请日：2012-07-09
- 公开(公告)号：KR101361546B1 公开(公告)日：2014-02-13
- 发明人： 김명규 , 나인섭 , 박상철
- 申请人： 전남대학교산학협력단
- 申请人地址： 광주광역시 북구 용봉로 ** (용봉동)
- 专利权人： 전남대학교산학협력단
- 当前专利权人： 전남대학교산학협력단
- 当前专利权人地址： 광주광역시 북구 용봉로 ** (용봉동)
- 代理人： 남충우; 노철호
- 主分类号： G06F19/00
- IPC分类号： G06F19/00 ; G06F19/10
The device that the computer program is a computer-readable medium and execute them in contained is provided. The computer program, to be able to perform a hereditary skeletal muscle ion channel disease causes predictable method to determine the cause of the genes of hereditary skeletal muscle ion channel disease using symptom information from accidental paralysis and dystonia syndrome, hereditary skeletal muscle ion channels listed in this medium quick genetic cause of the disease and be able to accurately predict. Thus, the user is able to examine only some genes of various causes genes to determine the cause of hereditary skeletal muscle ion channel disease, it is possible to determine the cause of hereditary skeletal muscle ion channel disease in a short time at low cost.