MTMR4 SNVs modulate ion channel degradation and clinical severity in congenital long QT syndrome: insights in the mechanism of action of protective modifier genes

por Lee, Yee-Ki, Sala, Luca, Mura, Manuela, Rocchetti, Marcella, Pedrazzini, Matteo, Ran, Xinru, Mak, Timothy S H, Crotti, Lia, Sham, Pak C, Torre, Eleonora, Zaza, Antonio, Schwartz, Peter J, Tse, Hung-Fat, Gnecchi, Massimiliano
Publicado 2020

Genetic Overlap Between Attention Deficit/Hyperactivity Disorder and Autism Spectrum Disorder in SHANK2 Gene

por Ma, Suk-Ling, Chen, Lu Hua, Lee, Chi-Chiu, Lai, Kelly Y. C., Hung, Se-Fong, Tang, Chun-Pan, Ho, Ting-Pong, Shea, Caroline, Mo, Flora, Mak, Timothy S. H., Sham, Pak-Chung, Leung, Patrick W. L.
Publicado 2021