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A null variant in PUS3 confirms its involvement in intellectual disability and further delineates the associated neurodevelopmental disease
Author(s) -
Abdelrahman Hanadi A.,
AlShamsi Aisha M.,
Ali Bassam R.,
AlGazali Lihadh
Publication year - 2018
Publication title -
clinical genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.543
H-Index - 102
eISSN - 1399-0004
pISSN - 0009-9163
DOI - 10.1111/cge.13443
Subject(s) - intellectual disability , disease , genetics , biology , medicine , developmental psychology , psychology
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