Diagnostic utility of transcriptome sequencing for rare Mendelian diseases
Hane Lee(University of California, Los Angeles), Alden Huang(University of California, Los Angeles), Lee-kai Wang(University of California, Los Angeles), Amanda J. Yoon(University of California, Los Angeles), Genecee Renteria(University of California, Los Angeles), Ascia Eskin(University of California, Los Angeles), Rebecca Signer(University of California, Los Angeles), Naghmeh Dorrani(University of California, Los Angeles), Shirley Nieves‐Rodriguez(University of California, Los Angeles), Jijun Wan(University of California, Los Angeles), Emilie D. Douine(University of California, Los Angeles), Jeremy D. Woods(University of California, Los Angeles), Esteban C. Dell’Angelica(University of California, Los Angeles), Brent L. Fogel(University of California, Los Angeles), Martín G. Martín(University of California, Los Angeles), Manish J. Butte(University of California, Los Angeles), Neil H. Parker(University of California, Los Angeles), Richard T. Wang(University of California, Los Angeles), Perry B. Shieh(University of California, Los Angeles), Derek A. Wong(University of California, Los Angeles), Natalie M. Gallant(University of California, Irvine), Kathryn Singh(University of California, Irvine), Yael Asher(Cedars-Sinai Medical Center), Janet S. Sinsheimer(University of California, Los Angeles), Deborah Krakow(University of California, Los Angeles), Sandra K. Loo(University of California, Los Angeles), Patrick Allard(University of California, Los Angeles), Jeanette C. Papp(University of California, Los Angeles), Christina G.S. Palmer(University of California, Los Angeles), Julián A. Martínez-Agosto(University of California, Los Angeles), Stanley F. Nelson(University of California, Los Angeles)
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