Novel missense mutation in the bZIP transcription factor, MAF, associated with congenital cataract, developmental delay, seizures and hearing loss (Aymé-Gripp syndrome).
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Novel missense mutation in the bZIP transcription factor, MAF, associated with congenital cataract, developmental delay, seizures and hearing loss (Aymé-Gripp syndrome).
description
2017 nî lūn-bûn
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2017 թուականի Մայիսին հրատարակուած գիտական յօդուած
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2017 թվականի մայիսին հրատարակված գիտական հոդված
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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
@zh-hk
2017年論文
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2017年論文
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2017年论文
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name
Novel missense mutation in the ...... ng loss (Aymé-Gripp syndrome).
@ast
Novel missense mutation in the ...... ng loss (Aymé-Gripp syndrome).
@en
type
label
Novel missense mutation in the ...... ng loss (Aymé-Gripp syndrome).
@ast
Novel missense mutation in the ...... ng loss (Aymé-Gripp syndrome).
@en
prefLabel
Novel missense mutation in the ...... ng loss (Aymé-Gripp syndrome).
@ast
Novel missense mutation in the ...... ng loss (Aymé-Gripp syndrome).
@en
P2093
P2860
P50
P1433
P1476
Novel missense mutation in the ...... ing loss (Aymé-Gripp syndrome)
@en
P2093
Kathryn P Burdon
Shari Javadiyan
Shiwani Sharma
Theresa Casey
P2860
P2888
P356
10.1186/S12881-017-0414-7
P577
2017-05-08T00:00:00Z
P6179
1085210947