disease 3,094 words KG: ent-dise-615bf469
Contents

Genetics of Progressive Supranuclear Palsy

Disease Info
H1 haplotype3-6x increased risk in homozygous individuals
STX6 genePrevious GWAS identified syntaxin-6 as a risk modifier
EIF2AK3Involved in unfolded protein response
MOBPMyelin-associated oligodendrocyte basic protein
SLCO1A2Solute carrier organic anion transporter
DatabasesOMIMOrphanetClinicalTrialsPubMed

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