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Homozygous protein C deficiency with purpura fulminans: report of a new case and a description of a novel mutation.
Blood Coagul Fibrinolysis. 2003 Apr;14(3):303-6. doi: 10.1097/01.mbc.0000061287.28953.2c.
Blood Coagul Fibrinolysis. 2003.
PMID: 12695756
A new autosomal recessive syndrome. Early onset of pancytopenia, distinct facial features, growth retardation and developmental delay.
Al-Batniji FS, Mahmoud MA, Van Dijken PJ, Al-Asiri RH, Al-Swaid AF, Al-Marshedy AM.
Al-Batniji FS, et al.
Saudi Med J. 2001 Dec;22(12):1122-6.
Saudi Med J. 2001.
PMID: 11802189
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