eP380: Sequencing of entire 2.2 MB DMD gene facilitates diagnostic testing and aids selection of patients for therapeutic intervention
Author(s) -
Babi Ramesh Reddy Nallamilli,
Naga Guruju,
Lakshmanan Jagannathan,
Vinish Ramachander,
Lora Bean,
Madhuri Hegde
Publication year - 2022
Publication title -
genetics in medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.509
H-Index - 128
eISSN - 1530-0366
pISSN - 1098-3600
DOI - 10.1016/j.gim.2022.01.415
Subject(s) - duchenne muscular dystrophy , medicine , newborn screening , muscular dystrophy , gene , genetic testing , creatine kinase , genetics , bioinformatics , pediatrics , biology
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