Article

The Italian National Registry for FSHD: An Enhanced Data Integration and an Analytics Framework Towards Smart Health Care and Precision Medicine for a Rare Disease

2021-05-04

Abstract excerpt

<title>Abstract</title> <p><bold>BACKGROUND</bold>The <italic>Italian Clinical network for FSHD</italic> (ICNF) has established the Italian National Registry for FSHD (INRF), collecting data from patients affected by Facioscapulohumeral dystrophy (FSHD) and their relatives. The INRF has gathered data from molecular analysis, clinical evaluation, anamnestic information, and family history from more than 3500 parti...

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Literature Corpus work: 0ed4d8ef-aab9-50fb-b495-2e7a34b93e9a
DOI: 10.21203/rs.3.rs-447106/v1

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