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安格尔曼

  • 网络Angelman

安格尔曼安格尔曼
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安格尔曼

Angelman

“安格尔曼(Angelman) 综合征” （因版权原因，此处图片删除。） E3连接酶 E6-AP 实际上是由人的UBE3A 基因所编码。UBE3…

例句：
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"The most interesting elements that will come out of this will be the justification and reasoning behind the ideas, " Angleman said.
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Despite their differences, Prader-Willi and Angelman are two sides of the same coin.
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Angelman syndrome is associated with a mutation on the mother's chromosome 15.
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One was identified in 1965 by English physician Harry Angelman, who was struck by the faces of three children he treated.
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Many children with Angelman syndrome never learn to speak or read.

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