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Mutations in IFT80 cause SRPS Type IV. Report of two families and review
Varoona Bizaoui1,2, Céline Huber3, Eva Kohaut4
1Reference Center for Skeletal Dysplasia, AP-HP, Necker-Enfants Malades Hospital, Paris, France.
Abstract:
We report novel causative mutations in the IFT80 gene identified in four fetuses from two unrelated families with Beemer-Langer syndrome (BLS) or BLS-like phenotypes. We discuss the implication of the IFT80 gene in ciliopathies, and its diagnostic value for BLS among other SRPS.
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