论文信息 - Broadening the phenotype of LRP2 mutations: a new mutation in LRP2 causes a predominantly ocular phenotype suggestive of Stickler syndrome - 字舞流文

Broadening the phenotype of LRP2 mutations: a new mutation in LRP2 causes a predominantly ocular phenotype suggestive of Stickler syndrome

G. Van Camp | F. Collins | M. Flaherty | J. Pinner | I. Schrauwen | M. Sommen | C. Claes | M. Flaherty | G. V. Camp | Charlotte Claes