All individuals with variants in gene GABRB3

10 entries on 1 page. Showing entries 1 - 10.
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00050492 - PubMed: DDDS 2015, Journal: DDDS 2015 family, 1 affected M - United Kingdom (Great Britain) - - - Decipher - ? seizures, global developmental delay, constipation 1 1 Johan den Dunnen
00089200 - PubMed: Epi4K consortium 2016, Journal: Epi4K consortium 2016 - M - - - - - - - EE epilepsy with myoclonic-atonic seizures 1 1 Johan den Dunnen
00089201 - PubMed: Epi4K consortium 2016, Journal: Epi4K consortium 2016 - M - - - - - - - EE Dravet syndrome like, seggregates with Generalized epilepsy with febrile seizures plus 1 1 Johan den Dunnen
00089202 - PubMed: Epi4K consortium 2016, Journal: Epi4K consortium 2016 - F - - - - - - - EE epileptic encephalopathy 1 1 Johan den Dunnen
00089203 - PubMed: Epi4K consortium 2016, Journal: Epi4K consortium 2016 - F - - - - - - - EE epileptic encephalopathy 1 1 Johan den Dunnen
00089204 - PubMed: Epi4K consortium 2016, Journal: Epi4K consortium 2016 - M - - - - - - - EE early-onset epileptic encephalopathy 1 1 Johan den Dunnen
00089205 - PubMed: Epi4K consortium 2016, Journal: Epi4K consortium 2016 - F - - - - - - - EE early-onset epileptic encephalopathy 1 1 Johan den Dunnen
00089206 - PubMed: Epi4K consortium 2016, Journal: Epi4K consortium 2016 - M - - - - - - - EE Lennox-Gastaut syndrome 1 1 Johan den Dunnen
00302774 1843.647 PubMed: Hamdan 2015 - M - Canada - - - - - ID moderate global developmental delay intellectual disability; speech words; not walking; epilepsy; autistic features; no microcephaly; no macrocephaly; MRI brain normal; no neurological abnormalities; no congenitial malformations; no cardiac malformations; no urogenitory abnormalities 1 1 Johan den Dunnen
00305976 Pat7 PubMed: Johannesen 2020 2-generation family, 1 affected, unaffected non-carrier parents F - Denmark - - - - - epilepsy - 1 1 Johan den Dunnen
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