Researchers have discovered vital insights into the genetic basis of a rare condition called type I CD36 deficiency. CD36 is a protein found on the surfaces of various cells, and its absence can lead to complications like platelet transfusion refractoriness and fetal and neonatal alloimmune thrombocytopenia. This study, using advanced DNA sequencing techniques, has identified key genetic variations and haplotypes that contribute to this deficiency, paving the way for better diagnosis and management of affected individuals. The findings highlight the power of haplotype analysis in uncovering the complex interplay between genetic factors and clinical phenotypes.
Decoding the CD36 Puzzle
CD36 is a multifunctional Click Here
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