All individuals with variants in gene GPT2

6 entries on 1 page. Showing entries 1 - 6.
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AscendingIndividual ID     

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00265401 GPT2-ID PubMed: Binaafar 2020 4-generation family, 4 affected sibs (3F, M), unaffected heterozygous carrier parents/relatives M yes Iran - 07y? - no none ID moderate intellectual disability (HP:0002342); no motor delay (-HP:0001270); mild speech delay (HP:0000750) 1 4 Ehsan Razmara
00265402 GPT2-ID1 - - M yes Iran - - - - - ID severe intellectual disability (HP:0010864); no motor delay (-HP:0001270); mild speech delay (HP:0000750) 1 1 Ehsan Razmara
00318011 PKMR281 PubMed: Riazuddin 2017 - - yes Pakistan - - - - - ID III:6: mild ID, speech delay, epilepsy; III:10 & III:11: slow learner & aggressive 1 1 Johan den Dunnen
00387868 M9000007 PubMed: Hu 2019 family, 2 affected individuals, first cousin parents - yes Iran Persia - - - - ID syndromic intellectual disability, microcephaly (SD-3.0), epilepsy 1 2 Johan den Dunnen
00426127 16SS2600 PubMed: Al-Kasbi 2022 patient, other affecteds in family F - Oman - - - - - ID - 1 1 Johan den Dunnen
00453034 Fam11 Journal: Paracha 2024 2-generation family, 2 affected brothers, heterozygous carrier parents/relatives M yes Pakistan - - - - - NDD severe intellectual disability, delayed developmental milestones with motor delay, speech problems, postnatal microcephaly, hypotonia, aggressive behaviour, spastic paraplegia (one patient) 1 2 Muhammad Umair
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