Novel variant c.1838A>G, p.(Gln613Arg) in NALCNcauses camptodactyly and cognitive delay : Clinical Dysmorphology

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Novel variant c.1838A>G, p.(Gln613Arg) in NALCNcauses camptodactyly and cognitive delay

Singh, Parshw; Agrawal, Neha; Maurya, Rajesh Kumar; Moirangthem, Amita

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Clinical Dysmorphology 31(4):p 206-210, October 2022. | DOI: 10.1097/MCD.0000000000000431
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