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Dijk, T. et al. (2018). Biallelic loss of function variants in COASY cause prenatal onset pontocerebellar hypoplasia, microcephaly, and arthrogryposis. European journal of human genetics. pp. 1752-1758. [Online].
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Dijk, T. et al. (2018). Biallelic loss of function variants in COASY cause prenatal onset pontocerebellar hypoplasia, microcephaly, and arthrogryposis. European journal of human genetics. pp. 1752-1758. [Online].