Compound Heterozygosity for Null Mutations and a Common Hypomorphic Risk Haplotype in TBX6 Causes Congenital Scoliosis. (Q51216598)
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| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Compound Heterozygosity for Null Mutations and a Common Hypomorphic Risk Haplotype in TBX6 Causes Congenital Scoliosis. |
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Compound Heterozygosity for Null Mutations and a Common Hypomorphic Risk Haplotype in TBX6 Causes Congenital Scoliosis. (English)
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Kazuki Takeda
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Ikuyo Kou
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Noriaki Kawakami
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Aritoshi Iida
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Masahiro Nakajima
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Yoji Ogura
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Eri Imagawa
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Noriko Miyake
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Naomichi Matsumoto
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Yukuto Yasuhiko
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Hideki Sudo
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Toshiaki Kotani
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Japan Early Onset Scoliosis Research Group
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Masaya Nakamura
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Morio Matsumoto
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Kota Watanabe
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Shiro Ikegawa
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5 January 2017
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38
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3
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317-323
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