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A rare missense variant in the ATP2C2 gene is associated with developmental language disorder (DLD)

Research output: Contribution to conference › Poster › peer-review

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Author(s)

A. Martinelli, M. Rice, S. Smith, J. Talcott, J. Stein, L. Kent, M. Hayiou-Thomas, D. Newbury, C. Hulme, S. Pitt, S. Paracchini

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Details

Original languageEnglish
Pages396-397
Number of pages2
Publication statusPublished - 1 Dec 2020
Event53rd European Society of Human Genetics (ESHG) Conference - Virtual
Duration: 6 Jun 2020 → 9 Jun 2020
Conference number: 53
https://2020.eshg.org/

Conference

Conference53rd European Society of Human Genetics (ESHG) Conference
Abbreviated titleESHG
Period6/06/20 → 9/06/20
Internet address

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  4. The DCDC2 deletion is not a risk factor for dyslexia

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  5. Copy number variation screen identifies a rare de novo deletion at chromosome 15q13.1-13.3 in a child with language impairment

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ID: 272681765

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