ribosomal protein uL3-like isoform X1 [Homo sapiens]

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Bi-allelic missense disease-causing variants in RPL3L associate neonatal dilated cardiomyopathy with muscle-specific ribosome biogenesis. [Hum Genet. 2020]
Bi-allelic missense disease-causing variants in RPL3L associate neonatal dilated cardiomyopathy with muscle-specific ribosome biogenesis.
Ganapathi M, Argyriou L, Martínez-Azorín F, Morlot S, Yigit G, Lee TM, Auber B, von Gise A, Petrey DS, Thiele H, et al. Hum Genet. 2020 Nov; 139(11):1443-1454. Epub 2020 Jun 8.
Exploring the Regulation and Function of Rpl3l in the Development of Early-Onset Dilated Cardiomyopathy and Congestive Heart Failure Using Systems Genetics Approach. [Genes (Basel). 2023]
Exploring the Regulation and Function of Rpl3l in the Development of Early-Onset Dilated Cardiomyopathy and Congestive Heart Failure Using Systems Genetics Approach.
Bajpai AK, Gu Q, Orgil BO, Alberson NR, Towbin JA, Martinez HR, Lu L, Purevjav E. Genes (Basel). 2023 Dec 29; 15(1). Epub 2023 Dec 29.
Categorized Genetic Analysis in Childhood-Onset Cardiomyopathy. [Circ Genom Precis Med. 2020]
Categorized Genetic Analysis in Childhood-Onset Cardiomyopathy.
Al-Hassnan ZN, Almesned A, Tulbah S, Alakhfash A, Alhadeq F, Alruwaili N, Alkorashy M, Alhashem A, Alrashdan A, Faqeih E, et al. Circ Genom Precis Med. 2020 Oct; 13(5):504-514. Epub 2020 Sep 1.

RefSeq mRNA
See reference mRNA sequence for the RPL3L gene (XM_011522571.3).
RefSeq protein isoforms
See 4 reference sequence protein isoforms for the RPL3L gene.

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Protein