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De novo 1p35.2 microdeletion including PUM1 identified in a patient with sporadic West syndrome
Author(s) -
Imaizumi Taichi,
Mogami Yukiko,
Okamoto Nobuhiko,
YamamotoShimojima Keiko,
Yamamoto Toshiyuki
Publication year - 2019
Publication title -
congenital anomalies
Language(s) - Uncategorized
Resource type - Journals
eISSN - 1741-4520
pISSN - 0914-3505
DOI - 10.1111/cga.12322
Subject(s) - genetics , biology , medicine , computer science
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