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Angius, A. et al. (2018). Novel NALCN biallelic truncating mutations in siblings with IHPRF1 syndrome. Clinical genetics. 93 (6), pp. 1245-1247. [Online].
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Angius, A. et al. (2018). Novel NALCN biallelic truncating mutations in siblings with IHPRF1 syndrome. Clinical genetics. 93 (6), pp. 1245-1247. [Online].