TRPM1 is mutated in patients with autosomal-recessive complete congenital stationary night blindness.
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T. Léveillard | J. Sahel | S. Jacobson | B. Lorenz | X. Guillonneau | E. Zrenner | W. Berger | S. Bhattacharya | D. Schorderet | M. Preising | V. Moskova-Doumanova | B. Wissinger | F. Munier | I. Audo | S. Mohand-Saïd | S. Kohl | U. Kellner | C. Hamel | B. Leroy | A. Renner | K. Bujakowska | E. Nandrot | A. Bernd | C. Poloschek | C. Zeitz | A. Antonio | I. Drumare | Marie‐Elise Lancelot | E. de Baere | S. Defoort‐Dhellemmes