Associated Papers
Novel NARS2 variants in a patient with early-onset status epilepticus: case study and literature review.
Yang N et al.
Bmc Pediatrics, 2024
38310242 (PubMed )
Supplement: 12887_2024_4553_MOESM1_ESM.xlsx › trio.hg38.filter
Human genetic adaptation related to cellular zinc homeostasis.
Roca-Umbert A et al.
Plos Genetics, 2023
Peptide ancestry informative markers in uterine neoplasms from women of European, African, and Asian ancestry.
Bateman NW et al.
Iscience, 2022
35036865 (PubMed )
Supplement: mmc2.xlsx › SupplementalTable1A
Clinical Implications of Single Nucleotide Polymorphisms in Diagnosis of Asthma and its Subtypes.
Park JS et al.
Yonsei Medical Journal, 2019
Whole Genome Sequencing in an Acrodermatitis Enteropathica Family from the Middle East.
Abu-Duhier F et al.
Dermatology Research and Practice, 2018
30174688 (PubMed )
Supplement: 1284568.f1.docx
Integrated mRNA and microRNA transcriptome sequencing characterizes sequence variants and mRNA-microRNA regulatory network in nasopharyngeal carcinoma model systems.
Szeto CY et al.
Febs Open Bio, 2014
24490137 (PubMed )
Supplement: mmc5.xlsx › coding
Select a paper to view details