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Individual Clinically Diagnosed with CHARGE Syndrome but with a Mutation in KMT2D, a Gene Associated with Kabuki Syndrome: A Case Report

By Sonoko Sakata, Satoshi Okada, Kohei Aoyama, Keiichi Hara, Chihiro Tani, Reiko Kagawa, Akari Utsunomiya-Nakamura, Shinichiro Miyagawa, Tsutomu Ogata, Haruo Mizuno and Masao Kobayashi
Publisher: Frontiers Media SA
Year: 2017
DOI identifier: 10.3389/fgene.2017.00210
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Provided by: MUCC (Crossref)
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