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Article

A large family from Argentina with prekallikrein deficiency due to a compound heterozygosis (T insertion in intron 7 and Asp558Glu in exon 15): prekallikrein Cordoba.

American journal of hematology - 1 May 2010

Girolami Antonio, Marun Sebastian, Vettore Silvia, Scaliter Gilda, Molina Angelica, Scarparo Pamela, Tabares Aldo, Lombardi Anna Maria

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 20301226
DOI: 10.1002/ajh.21654

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