A rare transcript homozygous variants in CLRN1(USH3A) causes Usher syndrome type 3 in a Chinese family.

Bibliographic Details
Published in:	Orphanet Journal of Rare Diseases Vol. 19; no. 1; pp. 1 - 13
Main Authors:	Wang, Suyang, Xu, Chen Yang, Zhu, Yiming, Ding, Wenjuan, Hu, Jieyu, Xu, Baicheng, Guo, Yufen, Liu, Xiaowen
Format:	Journal Article
Published:	BioMed Central 9/20/2024
Online Access:	View this record in EBSCOhost

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