Contribution of Whole-Genome Sequencing and Transcript Analysis to Decipher Retinal Diseases Associated with MFSD8 Variants
暂无分享，去创建一个
H. Dollfus | D. Schorderet | M. Todorova | V. Vaclavik | I. Meunier | C. Dhaenens | B. Bocquet | A. Le Moing | A. Devos | V. Pelletier | I. Drumare | V. Smirnov | O. Grunewald | Anaïs Poncet | S. Defoort‐Dhellemmes | F. Jobic | Anne-Gaëlle Le Moing