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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.

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Title: A novel case of two siblings harbouring homozygous variant in the NEUROG1 gene with autism as an additional phenotype: a case report.
Authors: Sheth, Frenny1 (AUTHOR) frenny.sheth@frige.co.in, Shah, Jhanvi1 (AUTHOR), Patel, Ketan2 (AUTHOR), Patel, Darshan3 (AUTHOR), Jain, Deepika4 (AUTHOR), Sheth, Jayesh1 (AUTHOR), Sheth, Harsh1 (AUTHOR) harsh.sheth@frige.co.in
Source: BMC Neurology. 1/16/2023, Vol. 23 Issue 1, p1-8. 8p.
Database: Academic Search Ultimate
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  Data: A novel case of two siblings harbouring homozygous variant in the NEUROG1 gene with autism as an additional phenotype: a case report.
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  Data: <searchLink fieldCode="AR" term="%22Sheth%2C+Frenny%22">Sheth, Frenny</searchLink><relatesTo>1</relatesTo> (AUTHOR)<i> frenny.sheth@frige.co.in</i><br /><searchLink fieldCode="AR" term="%22Shah%2C+Jhanvi%22">Shah, Jhanvi</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Patel%2C+Ketan%22">Patel, Ketan</searchLink><relatesTo>2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Patel%2C+Darshan%22">Patel, Darshan</searchLink><relatesTo>3</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Jain%2C+Deepika%22">Jain, Deepika</searchLink><relatesTo>4</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Sheth%2C+Jayesh%22">Sheth, Jayesh</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Sheth%2C+Harsh%22">Sheth, Harsh</searchLink><relatesTo>1</relatesTo> (AUTHOR)<i> harsh.sheth@frige.co.in</i>
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  Data: <searchLink fieldCode="JN" term="%22BMC+Neurology%22">BMC Neurology</searchLink>. 1/16/2023, Vol. 23 Issue 1, p1-8. 8p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=161326305
RecordInfo BibRecord:
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      – Type: doi
        Value: 10.1186/s12883-023-03065-1
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      – Code: eng
        Text: English
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      – TitleFull: A novel case of two siblings harbouring homozygous variant in the NEUROG1 gene with autism as an additional phenotype: a case report.
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            NameFull: Sheth, Frenny
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            NameFull: Shah, Jhanvi
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            NameFull: Patel, Ketan
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            NameFull: Jain, Deepika
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            NameFull: Sheth, Jayesh
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            – D: 16
              M: 01
              Text: 1/16/2023
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              Y: 2023
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