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Paganini, I. et al. (2017). A novel PAX1 null homozygous mutation in autosomal recessive otofaciocervical syndrome associated with severe combined immunodeficiency. Clinical genetics. 92 (6), pp. 664-668. [Online].
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Paganini, I. et al. (2017). A novel PAX1 null homozygous mutation in autosomal recessive otofaciocervical syndrome associated with severe combined immunodeficiency. Clinical genetics. 92 (6), pp. 664-668. [Online].