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HRA000617
   HRA000617.xlsx
Title:
Sequence and structure characteristics of 22 deletion breakpoints in intron 44 of DMD gene based on long-read sequencing
Release date:
2021-02-02
Description:
Exon deletions take up to 80% of mutations in DMD gene and intron 44 harbored more than 25% deletion start points. We investigated fine structures of breakpoints in intron 44 to find potential mechanisms of large deletions in intron 44 through Oxford Nanopore Sequencing.
Data Accessibility:   
Controlled access Request Data
BioProject:
PRJCA004385
Study type:
Disease Study
Disease name:
Duchenne muscular dystrophy
Data Access Committee

For each controlled access study, there is a corresponding Data Access Committee(DAC) to determine the access permissions. Access to actual data files is not managed by NGDC.


DAC NO.:
HDAC000390
DAC name:
DMD disease DAC
Contact person:
Dai Yi
Email:
pumchdy@pumch.cn
Description:
Duchenne and Becker muscular dystrophy DAC, Department of Neurology, Peking Union Medical College Hospital
Individuals & samples
Files
Request Data
Submitter:   Dai Yi / pumchdy@pumch.cn
Organization:   Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College
Submission date:   2021-01-29
Requests:   -