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		<title>腓骨肌萎缩症-病理分型-X-连锁遗传性腓骨肌萎缩症 - 版本历史</title>
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		<updated>2026-04-05T13:59:58Z</updated>
		<subtitle>本wiki的该页面的版本历史</subtitle>
		<generator>MediaWiki 1.30.0</generator>

	<entry>
		<id>http://120.24.161.253:5617/index.php?title=%E8%85%93%E9%AA%A8%E8%82%8C%E8%90%8E%E7%BC%A9%E7%97%87-%E7%97%85%E7%90%86%E5%88%86%E5%9E%8B-X-%E8%BF%9E%E9%94%81%E9%81%97%E4%BC%A0%E6%80%A7%E8%85%93%E9%AA%A8%E8%82%8C%E8%90%8E%E7%BC%A9%E7%97%87&amp;diff=1761080&amp;oldid=prev</id>
		<title>Admin：修改1</title>
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				<updated>2024-07-06T14:00:00Z</updated>
		
		<summary type="html">&lt;p&gt;修改1&lt;/p&gt;
&lt;table class=&quot;diff diff-contentalign-left&quot; data-mw=&quot;interface&quot;&gt;
				&lt;tr style=&quot;vertical-align: top;&quot; lang=&quot;zh-CN&quot;&gt;
				&lt;td colspan=&quot;1&quot; style=&quot;background-color: white; color:black; text-align: center;&quot;&gt;←上一版本&lt;/td&gt;
				&lt;td colspan=&quot;1&quot; style=&quot;background-color: white; color:black; text-align: center;&quot;&gt;2024年7月6日 (六) 14:00的版本&lt;/td&gt;
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&lt;/td&gt;&lt;/tr&gt;&lt;/table&gt;</summary>
		<author><name>Admin</name></author>	</entry>

	<entry>
		<id>http://120.24.161.253:5617/index.php?title=%E8%85%93%E9%AA%A8%E8%82%8C%E8%90%8E%E7%BC%A9%E7%97%87-%E7%97%85%E7%90%86%E5%88%86%E5%9E%8B-X-%E8%BF%9E%E9%94%81%E9%81%97%E4%BC%A0%E6%80%A7%E8%85%93%E9%AA%A8%E8%82%8C%E8%90%8E%E7%BC%A9%E7%97%87&amp;diff=1761081&amp;oldid=prev</id>
		<title>KGadmin：导入1个版本</title>
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				<updated>2024-07-06T13:03:26Z</updated>
		
		<summary type="html">&lt;p&gt;导入1个版本&lt;/p&gt;
&lt;table class=&quot;diff diff-contentalign-left&quot; data-mw=&quot;interface&quot;&gt;
				&lt;tr style=&quot;vertical-align: top;&quot; lang=&quot;zh-CN&quot;&gt;
				&lt;td colspan=&quot;1&quot; style=&quot;background-color: white; color:black; text-align: center;&quot;&gt;←上一版本&lt;/td&gt;
				&lt;td colspan=&quot;1&quot; style=&quot;background-color: white; color:black; text-align: center;&quot;&gt;2024年7月6日 (六) 13:03的版本&lt;/td&gt;
				&lt;/tr&gt;&lt;tr&gt;&lt;td colspan=&quot;2&quot; style=&quot;text-align: center;&quot; lang=&quot;zh-CN&quot;&gt;&lt;div class=&quot;mw-diff-empty&quot;&gt;（没有差异）&lt;/div&gt;
&lt;/td&gt;&lt;/tr&gt;&lt;/table&gt;</summary>
		<author><name>KGadmin</name></author>	</entry>

	<entry>
		<id>http://120.24.161.253:5617/index.php?title=%E8%85%93%E9%AA%A8%E8%82%8C%E8%90%8E%E7%BC%A9%E7%97%87-%E7%97%85%E7%90%86%E5%88%86%E5%9E%8B-X-%E8%BF%9E%E9%94%81%E9%81%97%E4%BC%A0%E6%80%A7%E8%85%93%E9%AA%A8%E8%82%8C%E8%90%8E%E7%BC%A9%E7%97%87&amp;diff=216409&amp;oldid=prev</id>
		<title>Admin：导入1个版本</title>
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				<updated>2021-10-21T07:57:15Z</updated>
		
		<summary type="html">&lt;p&gt;导入1个版本&lt;/p&gt;
&lt;table class=&quot;diff diff-contentalign-left&quot; data-mw=&quot;interface&quot;&gt;
				&lt;tr style=&quot;vertical-align: top;&quot; lang=&quot;zh-CN&quot;&gt;
				&lt;td colspan=&quot;1&quot; style=&quot;background-color: white; color:black; text-align: center;&quot;&gt;←上一版本&lt;/td&gt;
				&lt;td colspan=&quot;1&quot; style=&quot;background-color: white; color:black; text-align: center;&quot;&gt;2021年10月21日 (四) 07:57的版本&lt;/td&gt;
				&lt;/tr&gt;&lt;tr&gt;&lt;td colspan=&quot;2&quot; style=&quot;text-align: center;&quot; lang=&quot;zh-CN&quot;&gt;&lt;div class=&quot;mw-diff-empty&quot;&gt;（没有差异）&lt;/div&gt;
&lt;/td&gt;&lt;/tr&gt;&lt;/table&gt;</summary>
		<author><name>Admin</name></author>	</entry>

	<entry>
		<id>http://120.24.161.253:5617/index.php?title=%E8%85%93%E9%AA%A8%E8%82%8C%E8%90%8E%E7%BC%A9%E7%97%87-%E7%97%85%E7%90%86%E5%88%86%E5%9E%8B-X-%E8%BF%9E%E9%94%81%E9%81%97%E4%BC%A0%E6%80%A7%E8%85%93%E9%AA%A8%E8%82%8C%E8%90%8E%E7%BC%A9%E7%97%87&amp;diff=216404&amp;oldid=prev</id>
		<title>Admin：修改1</title>
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				<updated>2021-10-19T13:56:59Z</updated>
		
		<summary type="html">&lt;p&gt;修改1&lt;/p&gt;
&lt;p&gt;&lt;b&gt;新页面&lt;/b&gt;&lt;/p&gt;&lt;div&gt;主实体：[[腓骨肌萎缩症]]，关系：[[病理分型]] ，尾实体：[[X-连锁遗传性腓骨肌萎缩症]]&lt;br /&gt;
&lt;br /&gt;
实体ID:''605141''&lt;br /&gt;
==关系介绍==&lt;br /&gt;
待补充&lt;br /&gt;
&lt;br /&gt;
==来源==&lt;br /&gt;
===X-连锁遗传性腓骨肌萎缩症的研究进展（中华医学会文献）===&lt;br /&gt;
[[腓骨肌萎缩症]](CMT)是一组具有高度遗传异质性的周围神经系统单基因遗传病,多数呈常染色体显性遗传,X-连锁遗传性[[腓骨肌萎缩症]](CMTX)是第二常见类型.&lt;/div&gt;</summary>
		<author><name>Admin</name></author>	</entry>

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