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Article

Whole exome sequencing revealed biallelic IFT122 mutations in a family with CED1 and recurrent pregnancy loss.

Clinical genetics - 1 Jun 2014

Tsurusaki Y, Yonezawa R, Furuya M, Nishimura G, Pooh R K, Nakashima M, Saitsu H, Miyake N, Saito S, Matsumoto N

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PMID: 23826986
DOI: 10.1111/cge.12215

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