(Q55052729)
Statements
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Prenatal diagnosis of autosomal dominant hereditary spastic paraplegia (SPG42) caused by SLC33A1 mutation in a Chinese kindred. (English)
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Pengfei Lin
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Fei Mao
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Qiji Liu
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Chuanzhu Yan
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Yaoqin Gong
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1 May 2010
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30
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5
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485-486
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Identifiers
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