Filamin B mutations cause chondrocyte defects in skeletal development.
Lu J; Lian G; Lenkinski R; De Grand A; Vaid RR; Bryce T; Stasenko M; Boskey A; Walsh C; Sheen V; Human Molecular Genetics, 2007, vol. 16, issue 14, p 1661, ISSN 09646906. ISBN 09646906.

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