All individuals with variants in gene STT3B

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00385764 Fam2Pat2 PubMed: Shrimal 2013 4-generation family, 1 affected, unaffected heterozygous carrier parents/relatives M yes Iraq - 04y - - - CDG intrauterine growth retardation; 4y-deceased; microcephaly, failure to thrive, developmental delay, feeding problems, respiratory difficulties, intellectual disability, cerebellar atrophy, seizures/epilepsy, no visual tracking, optic nerve atrophy, hypotonia, gastrointestinal symptoms/G-Tube, liver involvement, thrombocytopenia; genital abnormalities, micropenis, hypoplastic scrotum, undescended testes 1 1 Johan den Dunnen
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