Comment on a 22-year follow-up reveals a variable disease severity in early-onset facioscapulohumeral dystrophy. This is the analysis of the clinical significance of molecular findings in subjects affected by early onset FSHD following a 22 year follow up.
Genotype-phenotype correlation: The ultimate challenge in facioscapolohumeral muscular dystrophy / Tupler, Rossella. - In: EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY. - ISSN 1090-3798. - 22:5(2018), pp. 737-737. [10.1016/j.ejpn.2018.07.010]
Genotype-phenotype correlation: The ultimate challenge in facioscapolohumeral muscular dystrophy
Tupler, Rossella
2018
Abstract
Comment on a 22-year follow-up reveals a variable disease severity in early-onset facioscapulohumeral dystrophy. This is the analysis of the clinical significance of molecular findings in subjects affected by early onset FSHD following a 22 year follow up.
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