Invention Grant
US09150923B2 Methods of identifying FHL1 mutations associated with novel X-linked muscular myopathies
有权
鉴定与新型X连锁肌肉肌病相关的FHL1突变的方法
- Patent Title: Methods of identifying FHL1 mutations associated with novel X-linked muscular myopathies
- Patent Title (中): 鉴定与新型X连锁肌肉肌病相关的FHL1突变的方法
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Application No.: US14077887Application Date: 2013-11-12
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Publication No.: US09150923B2Publication Date: 2015-10-06
- Inventor: John Vincent , Christian Windpassinger , Stefan Quasthoff
- Applicant: CENTRE FOR ADDICTION AND MENTAL HEALTH
- Applicant Address: CA Toronto, Ontario
- Assignee: Centre for Addiction and Mental Health
- Current Assignee: Centre for Addiction and Mental Health
- Current Assignee Address: CA Toronto, Ontario
- Agency: Winston & Strawn LLP
- Main IPC: C12Q1/68
- IPC: C12Q1/68 ; G01N33/566 ; G01N33/68 ; C07K14/47

Abstract:
Four and a Half LIM domains protein 1 (FHL-1) mutations at positions 128 or 224 that are associated with X-linked muscular myopathy, methods of screening subjects to identify those susceptible to muscular myopathy including muscular dystrophy and cardiomyopathy and kits.
Public/Granted literature
- US20140162259A1 FHL1 MUTATIONS ASSOCIATED WITH NOVEL X-LINKED MUSCULAR MYOPATHIES Public/Granted day:2014-06-12
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