The necdin interactome: evaluating the effects of amino acid substitutions and cell stress using proximity-dependent biotinylation (BioID) and mass spectrometry
Author:
Funder
Canadian Institutes of Health Research
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
Link
https://link.springer.com/content/pdf/10.1007/s00439-020-02193-9.pdf
Reference95 articles.
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3. Berger SI et al (2017) Exome analysis of Smith-Magenis-like syndrome cohort identifies de novo likely pathogenic variants. Hum Genet 136:409–420. https://doi.org/10.1007/s00439-017-1767-x
4. Berlanga JJ, Baass A, Sonenberg N (2006) Regulation of poly(A) binding protein function in translation: characterization of the Paip2 homolog, Paip2B. RNA 12:1556–1568. https://doi.org/10.1261/rna.106506
5. Bramswig NC et al (2017) Heterozygous HNRNPU variants cause early onset epilepsy and severe intellectual disability. Hum Genet 136:821–834. https://doi.org/10.1007/s00439-017-1795-6
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