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葡萄糖－6－磷酸脱氢酶缺乏症
葡萄糖－6－磷酸脱氢酶缺乏症
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葡萄糖－6－磷酸脱氢酶缺乏症
5 个讨论
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我是有G6PD病的显性，为何没有查出来？
冰蛋
• 最后回复
林家萘子
•
2023-12-20 01:16
5680
11
• 来自相关小组
女生，G6DP缺乏症一个风险突变，什么意思？
奋斗的FAT1基因
• 最后回复
元月十号
•
2023-07-24 20:15
1086
2
• 来自相关小组
，这算是怎么回事，严重吗？
很好的DACH1基因
• 最后回复
大灰狼
•
2022-02-17 15:30
1949
2
• 来自相关小组
我有蚕豆病，23魔方显示携带一个变异有风险这里却显示未携带……
克林斯曼
• 最后回复
逃跑的ARL4A基因
•
2021-08-24 00:39
3040
4
• 来自相关小组
为什么我患有g6pd缺乏症，却显示未携带这个基因
jbenjamin
• 最后回复
大灰狼
•
2021-08-23 11:54
4750
7
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发起讨论
葡萄糖－6－磷酸脱氢酶缺乏症
5 个讨论
相关基因
G6PD
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ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
ClinVar: public archive of interpretations of clinically relevant variants
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