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

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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Bibliographic Details
Main Authors: 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
Format: Article
Language:English
Published: Nature Portfolio 2025-07-01
Series:Scientific Reports
Subjects:
Full-length transcriptome sequencing
Waardenburg syndrome
Mitf
Pigmentation
Online Access:https://doi.org/10.1038/s41598-025-13359-8
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https://doi.org/10.1038/s41598-025-13359-8

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