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Compound heterozygosity for 2 novel TMEM16F mutations in a patient with Scott syndrome



Compound heterozygosity for 2 novel TMEM16F mutations in a patient with Scott syndrome



Blood 117(16): 4399-4400




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Accession: 052269071

Download citation: RISBibTeXText

PMID: 21511967

DOI: 10.1182/blood-2011-01-332502


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