Cite
HARVARD Citation
Kvarnung, M. et al. (2018). Genomic screening in rare disorders: New mutations and phenotypes, highlighting ALG14 as a novel cause of severe intellectual disability. Clinical genetics. 94 (6), pp. 528-537. [Online].
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Kvarnung, M. et al. (2018). Genomic screening in rare disorders: New mutations and phenotypes, highlighting ALG14 as a novel cause of severe intellectual disability. Clinical genetics. 94 (6), pp. 528-537. [Online].