The LAM Foundation urgently seeks to catalyze new treatments - and ultimately a cure - for LAM by advancing research, supporting compassionate care, and amplifying the voice of women with rare diseases.
To cite LAM Cell Atlas in your publications you can use the following reference:
1. Du Y, Guo M, Wu Y, Wagner A, Perl AK, Wikenheiser-Brokamp K, Yu J, Gupta N, Kopras E, Krymskaya V, Obraztsova K, Tang Y, Kwiatkowski D, Henske EP, McCormack F, Xu Y. Lymphangioleiomyomatosis (LAM) Cell Atlas. Thorax 2023;78(1):85-87. PMID:36599466.
