Pathogenic homozygous variations in ACTL6B cause DECAM syndrome: Developmental delay, Epileptic encephalopathy, Cerebral Atrophy, and abnormal Myelination
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Pathogenic homozygous variations in ACTL6B cause DECAM syndrome: Developmental delay, Epileptic encephalopathy, Cerebral Atrophy, and abnormal Myelination
description
2019 nî lūn-bûn
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2019年の論文
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2019年学术文章
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2019年学术文章
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2019年學術文章
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name
Pathogenic homozygous variatio ...... ophy, and abnormal Myelination
@en
type
label
Pathogenic homozygous variatio ...... ophy, and abnormal Myelination
@en
prefLabel
Pathogenic homozygous variatio ...... ophy, and abnormal Myelination
@en
P356
P1476
Pathogenic homozygous variatio ...... ophy, and abnormal Myelination
@en
P2093
Evren Gümüş
Merve Yazol
P304
P356
10.1002/AJMG.A.61210
P50
P577
2019-05-27T00:00:00Z