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HARVARD Citation
Alter, S. et al. (2018). Novel VPS33B mutation in a patient with autosomal recessive keratoderma‐ichthyosis‐deafness syndrome. American journal of medical genetics. 176 (12), pp. 2862-2866. [Online].
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Alter, S. et al. (2018). Novel VPS33B mutation in a patient with autosomal recessive keratoderma‐ichthyosis‐deafness syndrome. American journal of medical genetics. 176 (12), pp. 2862-2866. [Online].