Novel MASP1 mutations are associated with an expanded phenotype in 3MC1 syndrome

Overview of attention for article published in Orphanet Journal of Rare Diseases, September 2015

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New mutations identified in 3MC1 syndrome, severe rare autosomal recessive disorder http://t.co/FtdbW8tM3Z #OJRD #RareDisease

Novel MASP1 mutations are associated with an expanded phenotype in 3MC1 syndrome http://t.co/FanpAtRunm orphanetjournalofrarediseases

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