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2020
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Bi-allelic Loss-of-Function CACNA1B Mutations in Progressive Epilepsy-Dyskinesia.
Not available
S-EPMC6507039
|
biostudies-literature
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Multisystem Inflammatory Syndrome in U.S. Children and Adolescents.
Not available
S-EPMC7346765
|
biostudies-literature
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Evaluation of IFITM3 rs12252 Association With Severe Pediatric Influenza Infection.
Not available
S-EPMC5853450
|
biostudies-literature
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CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language.
Not available
S-EPMC6218476
|
biostudies-literature
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