Identification of a novel splicing‐altering LAMP2 variant in a Chinese family with Danon disease
Abstract Aims This study aimed to identify a novel splicing‐altering LAMP2 variant associated with Danon disease. Methods and results To identify the potential genetic mutation in a Chinese pedigree, whole‐exome sequencing was conducted in the proband, and Sanger sequencing was performed on the prob...
Main Authors: | , , , , |
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Format: | Article |
Language: | English |
Published: |
Wiley
2023-08-01
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Series: | ESC Heart Failure |
Subjects: | |
Online Access: | https://doi.org/10.1002/ehf2.14417 |