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The common A467T mutation in the human mitochondrial DNA polymerase (POLG) compromises catalytic efficiency and interaction with the accessory subunit.
Characteristics and Prevalence of Asthma/Chronic Obstructive Pulmonary Disease Overlap in the United States.
Spontaneous splenic rupture in a patient with factor XIII deficiency and a novel mutation.
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Spontaneous splenic rupture in a patient with factor XIII deficiency and a novel mutation.
Spontaneous splenic rupture in a patient with factor XIII deficiency and a novel mutation. Pediatr Blood Cancer. 2008 Jan; 50(1):113-4.
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PubMed
subject areas
Child
Factor XIII
Factor XIII Deficiency
Hemorrhagic Disorders
Humans
Male
Mutation
Rupture, Spontaneous
Splenic Rupture
authors with profiles
Miguel Raul Abboud