Associated Papers
Evidence of a genetic background predisposing to complex regional pain syndrome type 1.
Shaikh SS et al.
Journal of Medical Genetics, 2024
ANO10 Function in Health and Disease.
Chrysanthou A et al.
Cerebellum (london, England), 2023
A genome-wide association study identifies susceptibility loci for primary central nervous system lymphoma at 6p25.3 and 3p22.1: a LOC Network study.
Labreche K et al.
Neuro-oncology, 2019
Novel compound heterozygous MYO7A mutations in Moroccan families with autosomal recessive non-syndromic hearing loss.
Bakhchane A et al.
Plos One, 2017
28472130 (PubMed )
Supplement: pone.0176516.s002.xlsx › Feuil1
Ion channels in regulated cell death.
Kunzelmann K
Cellular and Molecular Life Sciences : Cmls, 2016
Modulating Ca²⁺ signals: a common theme for TMEM16, Ist2, and TMC.
Kunzelmann K et al.
Pflugers Archiv : European Journal of Physiology, 2016
A Coding Variant of ANO10, Affecting Volume Regulation of Macrophages, Is Associated with Borrelia Seropositivity.
Hammer C et al.
Molecular Medicine (cambridge, Mass.), 2015
How well do whole exome sequencing results correlate with medical findings? A study of 89 Mayo Clinic Biobank samples.
Middha S et al.
Frontiers in Genetics, 2015
26257771 (PubMed )
Supplement: Table12.XLSX › snv.tier2
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