Hidden Genetic Variation in LCA9‐Associated Congenital Blindness Explained by 5′UTR Mutations and Copy‐Number Variations of NMNAT1
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R. Veitia | M. De Bruyne | F. Coppieters | A. Todeschini | M. Kondo | F. Meire | C. van Cauwenbergh | B. Leroy | M. Ongenaert | T. Fujimaki | M. Bauwens | H. Verdin | A. Baert | Akira Murakami | E. de Baere | Annelot Baert | Anne-Laure Todeschini