Associated Papers
Full-length haplotype reconstruction of CD36 by long-read sequencing: uncovers a novel structural variant.
Liang S et al.
Bmc Genomics, 2026
Haplotypes analysis reveals the genetic basis of type I CD36 deficiency.
Xia W et al.
Scientific Reports, 2024
The polymorphism analysis for CD36 among platelet donors.
Lyu Q et al.
Scientific Reports, 2024
Frequency and molecular basis of CD36 deficiency among platelet donors in Kunming, China.
Lyu Q et al.
Platelets, 2023
Dendritic Spine in Autism Genetics: Whole-Exome Sequencing Identifying De Novo Variant of CTTNBP2 in a Quad Family Affected by Autism Spectrum Disorder.
Xie Y et al.
Children (basel, Switzerland), 2022
36670631 (PubMed )
Supplement: children-10-00080-s001.zip › children-2044403-supplementary › children-2044403-Supplementary › Supplementary_Tables-R1.xlsx › STS5
Frequency of CD36 deficiency in Thais analyzed by quantification of CD36 on cell surfaces and in plasma.
Phuangtham R et al.
Transfusion, 2020
Whole-exome Sequencing Helps the Diagnosis and Treatment in Children with Neurodevelopmental Delay Accompanied Unexplained Dyspnea.
Tong W et al.
Scientific Reports, 2018
29581464 (PubMed )
Supplement: 41598_2018_23503_MOESM1_ESM.xls › P22
Genetic variations of CD36 and low platelet CD36 expression - a risk factor for lipemic plasma donation in Taiwanese apheresis donors.
Lo SC et al.
Vox Sanguinis, 2016
Incidence and molecular basis of CD36 deficiency in Shanghai population.
Li R et al.
Transfusion, 2015
Variants of CD36 gene and their association with CD36 protein expression in platelets.
Xu X et al.
Blood Transfusion = Trasfusione Del Sangue, 2014
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