Whole-exome sequencing identifies a novel mutation of GPD1L (R189X) associated with familial conduction disease and sudden death.
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Whole-exome sequencing identifies a novel mutation of GPD1L (R189X) associated with familial conduction disease and sudden death.
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2017 nî lūn-bûn
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2017年の論文
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Whole-exome sequencing identif ...... tion disease and sudden death.
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Whole-exome sequencing identifies a novel mutation of GPD1L
@nl
type
label
Whole-exome sequencing identif ...... tion disease and sudden death.
@en
Whole-exome sequencing identifies a novel mutation of GPD1L
@nl
prefLabel
Whole-exome sequencing identif ...... tion disease and sudden death.
@en
Whole-exome sequencing identifies a novel mutation of GPD1L
@nl
P2093
P2860
P356
P1476
Whole-exome sequencing identif ...... ction disease and sudden death
@en
P2093
Jie-Yuan Jin
Jing-Jing Li
Liang-Liang Fan
Ya-Qin Chen
P2860
P304
P356
10.1111/JCMM.13409
P50
P577
2017-10-27T00:00:00Z