Biallelic sequence and structural variants in RAX2 are a novel cause for autosomal recessive inherited retinal disease
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J. van den Ende | M. McKibbin | C. Inglehearn | C. Toomes | M. Cortón | S. Banfi | F. Coppieters | J. de Zaeytijd | C. Ayuso | T. Cherry | Manir Ali | F. Testa | B. Leroy | F. Simonelli | F. Peelman | A. Torella | Stijn Van de Sompele | M. Karali | H. Verdin | Thalia Van Laethem | K. Khan | K. Van Schil | T. Rosseel | E. de Baere | Julien Derolez | Belen Jimenez | Claire E L Smith | S. Van de Sompele