Mutations in GPAA1, Encoding a GPI Transamidase Complex Protein, Cause Developmental Delay, Epilepsy, Cerebellar Atrophy, and Osteopenia.
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Mutations in GPAA1, Encoding a GPI Transamidase Complex Protein, Cause Developmental Delay, Epilepsy, Cerebellar Atrophy, and Osteopenia.
description
2017 nî lūn-bûn
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2017年の論文
@ja
2017年学术文章
@wuu
2017年学术文章
@zh-cn
2017年学术文章
@zh-hans
2017年学术文章
@zh-my
2017年学术文章
@zh-sg
2017年學術文章
@yue
2017年學術文章
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2017年學術文章
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name
Mutations in GPAA1, Encoding a ...... ellar Atrophy, and Osteopenia.
@en
Mutations in GPAA1, Encoding a ...... ellar Atrophy, and Osteopenia.
@nl
type
label
Mutations in GPAA1, Encoding a ...... ellar Atrophy, and Osteopenia.
@en
Mutations in GPAA1, Encoding a ...... ellar Atrophy, and Osteopenia.
@nl
prefLabel
Mutations in GPAA1, Encoding a ...... ellar Atrophy, and Osteopenia.
@en
Mutations in GPAA1, Encoding a ...... ellar Atrophy, and Osteopenia.
@nl
P2093
P2860
P50
P6366
P1154
2-s2.0-85033578776
P1476
Mutations in GPAA1, Encoding a ...... ellar Atrophy, and Osteopenia.
@en
P2093
Alexandra Bateman
Anik St-Denis
Christine Diggle
Christopher P Bennett
Clare V Logan
Colin A Johnson
Eamonn Sheridan
Elizabeth Berry-Kravis
Françoise Le Deist
P2860
P304
P356
10.1016/J.AJHG.2017.09.020
P407
P50
P5530
P577
2017-11-01T00:00:00Z
P6179
1092501723
P6366
2767058310