The discovery of novel mechanisms for lymphangioleiomyomatosis pathogenesis through GWAS: a rarity in rare respiratory disorders
2019
This is the largest genome-wide association study of risk for sporadic LAM, a rare genetic disorder, from an international effort which identified novel variants for LAM pathogenesis in a plausible gene, independent of variation in TSC1 and TSC2 http://bit.ly/2X0SeZ1
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