Whole-exome sequencing reveals POLR3B variants associated with progeria-related Wiedemann-Rautenstrauch syndrome

Wu, SW; Li, L; Feng, F; Wang, L; Kong, YY; Liu, XW; Yin, CH

Liu, XW (corresponding author), Capital Med Univ, Beijing Obstet & Gynecol Hosp, Dept Obstet, Beijing 100026, Chaoyang, Peoples R China.; Liu, XW; Yin, CH (corresponding author), Beijing Maternal & Child Hlth Care Hosp, Beijing 100026, Peoples R China.

ITALIAN JOURNAL OF PEDIATRICS, 2021; 47 (1):

Abstract

Background Wiedemann-Rautenstrauch syndrome (WRS) is a rare autosomal recessive neonatal progeroid disorder characterized by prenatal and postnatal gr......

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