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
Familial Temperature-Sensitive Auditory Neuropathy: Distinctive Clinical Courses Caused by Variants of the OTOF Gene.
Zhu YM et al.
Frontiers in Cell and Developmental Biology, 2021
34692690 (PubMed )
Supplement: Table_2.xlsx › Supplementary_Table_7
[Two Novel Mutations at the CD36 Gene Splicing Sites and Their Molecular Basis for the CD36 Deficiency].
Li LL et al.
Zhongguo Shi Yan Xue Ye Xue Za Zhi, 2020
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