Phenotype and Genotype of FXIII Deficiency in Two Unrelated Probands: Identification of a Novel F13A1 Large Deletion Mediated by Complex Rearrangement
Orphanet Journal of Rare Diseases - United Kingdom
doi 10.1186/s13023-019-1144-z
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Date
July 24, 2019
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Springer Science and Business Media LLC