Full length transcriptomic profiling reveals insights into the white coat phenotype in Waardenburg syndrome mice harboring the Mitf R324del mutation

Abstract Waardenburg syndrome (WS) is distinguished by depigmented patches of hair and skin, striking blue eyes and sensorineural hearing loss. Studies on alternative splicing (AS) in the abnormal pigmentation in skin in WS are currently poorly understood. In this study, we conducted comprehensive f...

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Autori principali:	Wei Gong, Lu Ma, Zhili Feng, Xiangyao Zeng, Lile Ouyang, Yihan Hu, Xianlin Liu, Jie Wen, Xiaoming Kang, Yalan Liu, Hong Wu, Qiancheng Jing, Chufeng He, Yong Feng
Natura:	Artigo
Lingua:	Inglês
Pubblicazione:	Nature Portfolio 2025-07-01
Serie:	Scientific Reports
Soggetti:	Full-length transcriptome sequencing Waardenburg syndrome Mitf Pigmentation
Accesso online:	https://doi.org/10.1038/s41598-025-13359-8
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