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

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

doi:10.1111/cge.12215

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

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

^*この論文の責任著者

研究成果: ジャーナルへの寄稿 › Letter › 査読

24 被引用数 (Scopus)

本文言語	英語
ページ（範囲）	592-594
ページ数	3
ジャーナル	Clinical Genetics
巻	85
号	6
DOI	https://doi.org/10.1111/cge.12215
出版ステータス	出版済み - 2014/06

ASJC Scopus 主題領域

遺伝学
遺伝学（臨床）

文献へのアクセス

10.1111/cge.12215

引用スタイル

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title = "Whole exome sequencing revealed biallelic IFT122 mutations in a family with CED1 and recurrent pregnancy loss",

author = "Y. Tsurusaki and R. Yonezawa and M. Furuya and G. Nishimura and Pooh, {R. K.} and M. Nakashima and H. Saitsu and N. Miyake and S. Saito and N. Matsumoto",

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AU - Tsurusaki, Y.

AU - Yonezawa, R.

AU - Furuya, M.

AU - Nishimura, G.

AU - Pooh, R. K.

AU - Nakashima, M.

AU - Saitsu, H.

AU - Miyake, N.

AU - Saito, S.

AU - Matsumoto, N.

PY - 2014/6

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JO - Clinical Genetics

JF - Clinical Genetics

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