Whole‐exome sequencing identifies a donor splice‐site...

  • Main
  • 2019 / 09
  • Whole‐exome sequencing identifies a donor splice‐site...
Molecular Genetics & Genomic Medicine 2019 / 09

Whole‐exome sequencing identifies a donor splice‐site variant in SMPX that causes rare X‐linked congenital deafness

Lv, Yuan, Gu, Jia, Qiu, Hao, Li, Huan, Zhang, Zhitao, Yin, Shaowei, Mao, Yan, Kong, Lingyin, Liang, Bo, Jiang, Hongkun, Liu, Caixia
How much do you like this book?
What’s the quality of the file?
Download the book for quality assessment
What’s the quality of the downloaded files?
Journal:
Molecular Genetics & Genomic Medicine
DOI:
10.1002/mgg3.967
Date:
September, 2019
File:
PDF, 1.35 MB
2019
Conversion to is in progress
Conversion to is failed