1 | HECW2, NDHSAL
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| Association of HECW2 variants with developmental and epileptic encephalopathy and knockdown of zebrafish hecw2a
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| Lu Q, Zhang MN, Shi XY, Zhang LQ, Wang YY, Liu LY, He W, Chen HM, He B, Zou LP.
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| Am J Med Genet A. Feb;185(2):377-383. doi: 10.1002/ajmg.a.61958. Epub 2020 Nov 18. 2021
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2 | HECW2, NDHSAL
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| De novo missense variants in HECW2 are associated with neurodevelopmental delay and hypotonia
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| Berko ER, Cho MT, Eng C, Shao Y, Sweetser DA, Waxler J, Robin NH, Brewer F, Donkervoort S, Mohassel P, Bönnemann CG, Bialer M, Moore C, Wolfe LA, Tifft CJ, Shen Y, Retterer K, Millan F, Chung WK.
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| J Med Genet. Feb;54(2):84-86. doi: 10.1136/jmedgenet-2016-103943. Epub 2016 Jul 7. 2017
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3 | HECW2, NDHSAL
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| Mutations in HECW2 are associated with intellectual disability and epilepsy.
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| Halvardson J, Zhao JJ, Zaghlool A, Wentzel C, Georgii-Hemming P, Månsson E, Ederth Sävmarker H, Brandberg G, Soussi Zander C, Thuresson AC, Feuk L.
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| J Med Genet. Oct;53(10):697-704. doi: 10.1136/jmedgenet-2016-103814. Epub 2016 Jun 22. 2016
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