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Fig. 4 | BMC Neurology

Fig. 4

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

Fig. 4

Schematic representation of (A) STRING interaction network of the NEUROG1 protein. (B) NEUROG1 gene along with the corresponding domains and variants observed till date. Variant highlighted in red corresponds to the present case. Solid line extending with dotted arrows indicates the large deletion encompassing the NEUROG1 gene and beyond

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BMC Neurology

ISSN: 1471-2377

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