Correspondence on “Deep phenotyping of 11 individuals with pathogenic variants in RNU4-2 reveals a clinically recognizable syndrome” by Valenzuela et al

Genetics in Medicine 2026 Open access

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Authors: Zarnab Saleem, Jawairya Muhammad Hussain, Qurat-ul-Ain Siddiqui, Sarah Zuberi

DOI: 10.1016/j.gim.2026.101686

Cited by: 1

References: 3

Fields of Study & Subjects

Genomics and Rare Diseases Hereditary Neurological Disorders Nuclear Structure and Function

References 3