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A novel single amino acid deletion impairs fibronectin function and causes familial glomerulopathy with fibronectin deposits: case report of a family

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Academic year: 2020

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Figure

Fig. 1 Renal histological and ultrastructural findings in the child (a, c, e, g, i, k, m and o) and his father (b, d, f, h, j, l, n, p), affected byGlomerulopathy with Fibronectin Deposits
Fig. 2 Superimposition between the native (white) and mutated (bronze) FN3 domain models

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