MOLECULAR DIAGNOSIS OF FSHD BY EPIGENETIC SIGNATURE
摘要
The present invention includes methods of determining whether an individual in need thereof has, or is at risk of developing, facioscapulohumeral muscular dystrophy (FSHD).
申请公布号
WO2016057648(A1)
申请公布日期
2016.04.14
申请号
WO2015US54462
申请日期
2015.10.07
申请人
UNIVERSITY OF MASSACHUSETTS MEDICAL CENTER
发明人
JONES, PETER, L.;JONES, TAKAKO;SALAMEH, JOHNNY;QUINN, COLIN;KING, OLIVER, D.
