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AutoCaSc: Prioritizing candidate genes for neurodevelopmental disorders.
Hum Mutat. 2022 Dec;43(12):1795-1807. doi: 10.1002/humu.24451. Epub 2022 Sep 14.
Hum Mutat. 2022.
PMID: 35998261
Bi-allelic loss of function variants in SLC30A5 as cause of perinatal lethal cardiomyopathy.
Lieberwirth JK, Joset P, Heinze A, Hentschel J, Stein A, Iannaccone A, Steindl K, Kuechler A, Abou Jamra R.
Lieberwirth JK, et al.
Eur J Hum Genet. 2021 May;29(5):808-815. doi: 10.1038/s41431-020-00803-8. Epub 2021 Feb 5.
Eur J Hum Genet. 2021.
PMID: 33547425
Free PMC article.
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Correction: Bi-allelic loss of function variants in SLC30A5 as cause of perinatal lethal cardiomyopathy.
Lieberwirth JK, Joset P, Heinze A, Hentschel J, Stein A, Iannaccone A, Steindl K, Kuechler A, Jamra RA.
Lieberwirth JK, et al.
Eur J Hum Genet. 2021 May;29(5):887. doi: 10.1038/s41431-021-00843-8.
Eur J Hum Genet. 2021.
PMID: 33750920
Free PMC article.
No abstract available.
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