Two novel mutations in the prothrombin gene identified in a patient with compound heterozygous type 1/2 prothrombin deficiency-Reference-Cited by-同舟云学术

Two novel mutations in the prothrombin gene identified in a patient with compound heterozygous type 1/2 prothrombin deficiency

Author:

Kuijper P. H. M.¹,Schellings M. W. M.¹,van de Kerkhof D.²,Nicolaes G. A. F.³,Reitsma P.⁴,Halbertsma F.⁵,Dors N.⁶

Affiliation:

1. Department of Clinical Chemistry; Máxima Medical Centre Veldhoven; Veldhoven; The Netherlands

2. Department of Clinical Chemistry; Catharina Hospital Eindhoven; Eindhoven; The Netherlands

3. Biochemistry Department; Cardiovascular Research Institute Maastricht; Maastricht University; Maastricht; The Netherlands

4. Department of Molecular Biology; Leiden University Medical Center; Leiden; The Netherlands

5. Department of Pediatrics; Máxima Medical Centre Veldhoven; Veldhoven; The Netherlands

6. Department of Pediatrics; Catharina Hospital Eindhoven; Eindhoven; The Netherlands

Publisher

Wiley

Subject

Genetics (clinical),Hematology,General Medicine

Link

Reference5 articles.

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