All individuals with variants in gene EXOC8

3 entries on 1 page. Showing entries 1 - 3.
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00413435 family PubMed: Ullah 2022 5-generation family, 6 affected (3F, 3M), unaffected heterozygous carrier parents/relatives F;M yes Pakistan - - - - - NDD see paper; ..., neurodevelopmental disorder, microcephaly, mandibular hypoplasia, weakness of muscles, malocclusion of teeth, drooling of saliva, urinary incontinence 1 1 Johan den Dunnen
00413436 FamV PubMed: Coulter 2020 5-generation family, 3 affected sisters, unaffected heterozygous carrier parents/relatives F yes - - - - - - ? see paper; ..., global developmental delay with regression, seizures, microcephaly 1 3 Johan den Dunnen
00426182 10MS2400 PubMed: Al-Kasbi 2022 patient, other affecteds in family M yes Oman - - - - - ID Severe acquired microcephaly, severe delay, seizures, optic nerve atrophy, and hypotonia 1 1 Johan den Dunnen
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