The intronic ABCA4 c.5461‐10T>C variant, frequently seen in patients with Stargardt disease, causes splice defects and reduced ABCA4 protein level
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G. Houge | P. Knappskog | S. Berland | E. Rødahl | I. Aukrust | C. Bredrup | Ragnhild W Jansson | Agnete Jørgensen | M. Haug | H. E. Rusaas | Hilde E. Rusaas | Per M. Knappskog