A homozygous loss-of-function CAMK2A mutation causes growth delay, frequent seizures and severe intellectual disability.
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A homozygous loss-of-function CAMK2A mutation causes growth delay, frequent seizures and severe intellectual disability.
description
2018 nî lūn-bûn
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2018年の論文
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2018年学术文章
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2018年学术文章
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2018年学术文章
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2018年学术文章
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2018年学术文章
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2018年學術文章
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2018年學術文章
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2018年學術文章
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name
A homozygous loss-of-function ...... evere intellectual disability.
@en
A homozygous loss-of-function ...... evere intellectual disability.
@nl
type
label
A homozygous loss-of-function ...... evere intellectual disability.
@en
A homozygous loss-of-function ...... evere intellectual disability.
@nl
prefLabel
A homozygous loss-of-function ...... evere intellectual disability.
@en
A homozygous loss-of-function ...... evere intellectual disability.
@nl
P2093
P2860
P50
P356
P1433
P1476
A homozygous loss-of-function ...... severe intellectual disability
@en
P2093
Ascia Eskin
Carine Bonnard
Kagistia Hana Utami
Mohammad El-Khateeb
Mohammad Shboul
Mohammed Al-Raqad
Ruizhu Zeng
Samah Al-Tawalbeh
Stanley F Nelson
P2860
P356
10.7554/ELIFE.32451
P407
P577
2018-05-22T00:00:00Z