Whole exome sequencing in congenital pain insensitivity identifies a novel causative intronic NTRK1-mutation due to uniparental disomy.
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Whole exome sequencing in congenital pain insensitivity identifies a novel causative intronic NTRK1-mutation due to uniparental disomy.
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2016 nî lūn-bûn
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2016年の論文
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2016年学术文章
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2016年学术文章
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2016年学术文章
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2016年学术文章
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@zh-sg
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@yue
2016年學術文章
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2016年學術文章
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name
Whole exome sequencing in cong ...... ion due to uniparental disomy.
@en
Whole exome sequencing in cong ...... ion due to uniparental disomy.
@nl
type
label
Whole exome sequencing in cong ...... ion due to uniparental disomy.
@en
Whole exome sequencing in cong ...... ion due to uniparental disomy.
@nl
prefLabel
Whole exome sequencing in cong ...... ion due to uniparental disomy.
@en
Whole exome sequencing in cong ...... ion due to uniparental disomy.
@nl
P2093
P2860
P356
P1476
Whole exome sequencing in cong ...... ion due to uniparental disomy.
@en
P2093
Cecilia Tomni
Kurt Gremel
Manuela Baumgartner
Maria Schabhüttl
Reinhard Windhager
Thomas Wieland
Tim M Strom
P2860
P304
P356
10.1002/AJMG.B.32458
P577
2016-05-17T00:00:00Z