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A novel case of two siblings harbouring homozygous variant in the NEUROG1 gene with autism as an additional phenotype: a case report

Document Type

Article

Author

Sheth, F.; Shah, J.; Sheth, J.; Sheth, H.; Patel, K.; Patel, D.; Jain, D.

Source

In: BMC Neurology. (BMC Neurology, December 2023, 23(1))

Subject

Language

English

ISSN

14712377

Online Access

EBSCOHost PDF Full Text (ProQuest Central) Full Text (Gale Academic Onefile) Open Access (BioMed Central) Web of Science JCR 저널정보 Scopus Find it@PNU

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