A genetic and clinical study of individuals with nonsyndromic retinopathy consequent upon sequence variants in HGSNAT, the gene associated with Sanfilippo C mucopolysaccharidosis
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W. Zein | O. Mahroo | G. Arno | M. Michaelides | A. Webster | S. Tuupanen | K. Pierpoint | A. Robson | E. Schiff | M. Varela | R. Ba-Abbad | S. Nutan | E. Ullah | L. Huryn | D. Burke | K. Harvey | R. Hufnagel | Laryssa A. Huryn