Premium
PUM1 haploinsufficiency is associated with syndromic neurodevelopmental delay and epilepsy
Author(s) -
Voet Julie,
Ceulemans Berten,
Kooy Frank,
Meuwissen Marije E. C.
Publication year - 2020
Publication title -
american journal of medical genetics part a
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.064
H-Index - 112
eISSN - 1552-4833
pISSN - 1552-4825
DOI - 10.1002/ajmg.a.61463
Subject(s) - medical genetics , pediatric neurology , university hospital , medicine , pediatrics , family medicine , genetics , biology , gene
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom