Publication | Closed Access
A Female Patient with Incomplete Hemophagocytic Lymphohistiocytosis Caused by a Heterozygous XIAP Mutation Associated with Non-Random X-Chromosome Inactivation Skewed Towards the Wild-Type XIAP Allele
39
Citations
20
References
2015
Year
Genetic DisorderHematologyPathologyWild-type Xiap AlleleInborn Error Of ImmunityFemale PatientIncomplete Hemophagocytic Lymphohistiocytosis
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