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T

Talia Akram

Uppsala University
H指数:5
被引数:137

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Monoallelic and bi-allelic variants in NCDN cause neurodevelopmental delay, intellectual disability, and epilepsy (vol 108, pg 739, 2021)
2022-03-010
OAAI
Monoallelic and bi-allelic variants in NCDN cause neurodevelopmental delay, intellectual disability, and epilepsy
2021-04-0116
OAAI
Mutations of KIF14 cause primary microcephaly by impairing cytokinesis
2017-10-1467
PREAI