Autor: Tomer Poleg
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<i>NSMCE2 / MMS21</i> structural variant causes chromosome breakage syndrome with primordial dwarfism and severe lung disease
European Journal of Human Genetics, Published online: 21 September 2026; doi:10.1038/s41431-026-02222-7NSMCE2 / MMS21 structural variant causes chromosome breakage syndrome with primordial dwarfism and severe lung disease
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<i>NSMCE2 / MMS21</i> structural variant causes chromosome breakage syndrome with primordial dwarfism and severe lung disease
European Journal of Human Genetics, Published online: 21 September 2026; doi:10.1038/s41431-026-02222-7NSMCE2 / MMS21 structural variant causes chromosome breakage syndrome with primordial dwarfism and severe lung disease