A novel mechanism for variable phenotypic expressivity in Mendelian diseases uncovered by an AU-rich element (ARE)-creating mutation.
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P2860
A novel mechanism for variable phenotypic expressivity in Mendelian diseases uncovered by an AU-rich element (ARE)-creating mutation.
description
2017 nî lūn-bûn
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2017年の論文
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2017年論文
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2017年論文
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2017年論文
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2017年論文
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2017年論文
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2017年论文
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2017年论文
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2017年论文
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name
A novel mechanism for variable ...... ement (ARE)-creating mutation.
@en
A novel mechanism for variable ...... ncovered by an AU-rich element
@nl
type
label
A novel mechanism for variable ...... ement (ARE)-creating mutation.
@en
A novel mechanism for variable ...... ncovered by an AU-rich element
@nl
prefLabel
A novel mechanism for variable ...... ement (ARE)-creating mutation.
@en
A novel mechanism for variable ...... ncovered by an AU-rich element
@nl
P2093
P2860
P1433
P1476
A novel mechanism for variable ...... ement (ARE)-creating mutation.
@en
P2093
Arif O Khan
Balsam M AlMaarik
Eman Alobeid
Firdous Abdulwahab
Khalid S A Khabar
Maher Al-Saif
Mais Hashem
Mohamed Abouelhoda
Niema Ibrahim
Nisha Patel
P2860
P2888
P356
10.1186/S13059-017-1274-3
P577
2017-07-28T00:00:00Z
P6179
1090912957