Extreme Phenotypic Variability of ACTG1‐Related Disorders in Hearing Loss by Maria T. Bernardi, Memoona Ramzan, Laura Calderon, Franco Salvatore, Maria Agustina De Rosa, Stephanie Bivona, Romina Armando, Natalia Vazquez, Maria Esnaola Azcoiti, Marcelo A. Marti, Claudia Arberas, Maria Gabriela Ropelato, Silvina Olha, Byron L. Lam, Fred F. Telischi, Mustafa Tekin, Katherina Walz

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Actin gamma 1 is a critical regulator of pancreatic ductal adenocarcinoma by Yichen Tang, Xuehui Peng, Xiaobing Huang, Jing Li

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Ocular findings in Baraitser–Winter syndrome with a de novo mutation in the ACTG1 gene: a case report by Jae Won Kim, Sook-Young Kim, Donghun Lee

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HMBA ameliorates obesity by MYH9‐ and ACTG1‐dependent regulation of hypothalamic neuropeptides by Seokjae Park, Sungjoon Oh, Nayoun Kim, Eun‐Kyoung Kim

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MBD3 promotes epithelial-mesenchymal transition in gastric cancer cells by upregulating ACTG1 via the PI3K/AKT pathway by Huizhi Wang, Jingyu Min, Yuntao Ding, Zhengyue Yu, Yujing Zhou, Shunyu Wang, Aihua Gong, Min Xu

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DFNA20/26 and Other ACTG1-Associated Phenotypes: A Case Report and Review of the Literature by Ugo Sorrentino, Chiara Piccolo, Chiara Rigon, Valeria Brasson, Eva Trevisson, Francesca Boaretto, Alessandro Martini, Matteo Cassina

Subjects: “…<i>ACTG1</i>…”
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When Familial Hearing Loss Means Genetic Heterogeneity: A Model Case Report by Camille Cenni, Luke Mansard, Catherine Blanchet, David Baux, Christel Vaché, Corinne Baudoin, Mélodie Moclyn, Valérie Faugère, Michel Mondain, Eric Jeziorski, Anne-Françoise Roux, Marjolaine Willems

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