Homo sapiens putative open reading frame; duplicate of the functional - Nucleotide

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Genome-wide CRISPR screens identify novel regulators of wild-type and mutant p53 stability. [Mol Syst Biol. 2024]
Genome-wide CRISPR screens identify novel regulators of wild-type and mutant p53 stability.
Lü Y, Cho T, Mukherjee S, Suarez CF, Gonzalez-Foutel NS, Malik A, Martinez S, Dervovic D, Oh RH, Langille E, et al. Mol Syst Biol. 2024 Jun; 20(6):719-740. Epub 2024 Apr 5.
Clinical Phenotype of Pediatric and Adult Patients With Spinal Muscular Atrophy With Four SMN2 Copies: Are They Really All Stable? [Ann Neurol. 2023]
Clinical Phenotype of Pediatric and Adult Patients With Spinal Muscular Atrophy With Four SMN2 Copies: Are They Really All Stable?
Ricci M, Cicala G, Capasso A, Coratti G, Fiori S, Cutrona C, D'Amico A, Sansone VA, Bruno C, Messina S, et al. Ann Neurol. 2023 Dec; 94(6):1126-1135. Epub 2023 Sep 22.
The Carrier Frequency of Two SMN1 Genes in Parents of Symptomatic Children with SMA and the Significance of SMN1 Exon 8 in Carriers. [Genes (Basel). 2023]
The Carrier Frequency of Two SMN1 Genes in Parents of Symptomatic Children with SMA and the Significance of SMN1 Exon 8 in Carriers.
Davidson JE, Russell JS, Martinez NN, Mowat DR, Jones KJ, Kirk EP, Kariyawasam D, Farrar M, D'Silva A. Genes (Basel). 2023 Jul 6; 14(7). Epub 2023 Jul 6.

Homo sapiens putative open reading frame; duplicate of the functional spinal mus...
Homo sapiens putative open reading frame; duplicate of the functional spinal muscular atrophy gene, cDNA clone BCD514, GenBank Accession Number U18423; it is not known if this copy of the gene is actually translated mRNA, partial cds
gi|736410|gb|U21914.1|HSU21914

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Nucleotide