Cell-type-specific profiling of human cellular models of fragile X syndrome reveal PI3K-dependent defects in translation and neurogenesis
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Chadwick M. Hales | P. Jin | S. Warren | E. Klann | Marius Wernig | J. Taliaferro | E. Berry-Kravis | V. Martínez‐Cerdeño | Ying Zhou | Samuele G. Marro | G. Bassell | Z. Wen | Feiran Zhang | C. Hales | M. Kalinowska | Z. McEachin | Nisha Raj | M. Wolf-Ochoa | Megan E. Merritt-Garza | William Harousseau | Lu Chen | Zachary T. McEachin