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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

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PMID: 21511967

DOI: 10.1182/blood-2011-01-332502

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