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De novo ATP1A3 and compound heterozygous NLRP3 mutations in a child with autism spectrum disorder, episodic fatigue and somnolence, and muckle-wells syndrome
PaperCitations, authors & open-access status
De novo ATP1A3 and compound heterozygous NLRP3 mutations in a child with autism spectrum disorder, episodic fatigue and somnolence, and muckle-wells syndrome is a paper indexed in ScholarIQ from OpenAlex. ScholarIQ records 19 citations, 2018 year and gold oa status.
19
Citations
2018
Year
gold
OA Status