A novel nucleotide oligomerisation domain 2 mutation in a family with Blau syndrome: Phenotype and function.
about
A novel nucleotide oligomerisation domain 2 mutation in a family with Blau syndrome: Phenotype and function.
description
2017 nî lūn-bûn
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2017年の論文
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2017年学术文章
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2017年学术文章
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2017年学术文章
@zh-cn
2017年学术文章
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2017年学术文章
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2017年学术文章
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2017年學術文章
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2017年學術文章
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name
A novel nucleotide oligomerisa ...... drome: Phenotype and function.
@en
A novel nucleotide oligomerisa ...... drome: Phenotype and function.
@nl
type
label
A novel nucleotide oligomerisa ...... drome: Phenotype and function.
@en
A novel nucleotide oligomerisa ...... drome: Phenotype and function.
@nl
prefLabel
A novel nucleotide oligomerisa ...... drome: Phenotype and function.
@en
A novel nucleotide oligomerisa ...... drome: Phenotype and function.
@nl
P2093
P2860
P356
P1433
P1476
A novel nucleotide oligomerisa ...... ndrome: Phenotype and function
@en
P2093
Dorota Rowczenio
Eddy Fischer
John B Ziegler
Ming Wei Lin
P2860
P304
P356
10.1177/1753425917727063
P577
2017-08-24T00:00:00Z