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Vivero, M. et al. (2017). Additional de novo missense genetic variants in NALCN associated with CLIFAHDD syndrome. Clinical genetics. 91 (6), pp. 929-931. [Online].
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Vivero, M. et al. (2017). Additional de novo missense genetic variants in NALCN associated with CLIFAHDD syndrome. Clinical genetics. 91 (6), pp. 929-931. [Online].