论文信息 - Mutations in SDCCAG8/NPHP10 Cause Bardet-Biedl Syndrome and Are Associated with Penetrant Renal Disease and Absent Polydactyly - 字舞流文

Mutations in SDCCAG8/NPHP10 Cause Bardet-Biedl Syndrome and Are Associated with Penetrant Renal Disease and Absent Polydactyly

N. Katsanis | A. Toutain | C. Redin | H. Dollfus | M. Gérard | M. Fischbach | C. Stoetzel | J. Muller | L. Perrin | E. Schaefer | J. Lauer | F. Stutzmann | S. Caillard | V. Marion | M. Durand | V. B. Greene | J. Letsch | D. Christmann | A. Zaloszyc | V. Bennouna Greene | Y. Perdomo-Trujillo | E. Schaefer | R.A. Lewis | X. Bei | M. Kribs | C. Mutter | Xiaoshu Bei | R. Lewis | Julia Lauer