All individuals with variants in gene STXBP5L

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00034216 family PubMed: Kumar 2015, PubMed: Kumar 2015, PubMed: Kumar 2022 3-generation family, 2 affected sibs (F, M), unaffected heterozygous carrier parents/sibs F;M yes - Middle East - - - - neurodegeneration see paper; infantile-onset neurodegenerative disorder, predominant sensorimotor axonal neuropathy, optic atrophy, cognitive deficit 1 2 Johan den Dunnen
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