Buchert, R., Nesbitt, A. I., Tawamie, H., Krantz, I. D., Medne, L., Helbig, I., . . . Abou Jamra, R. (2016). SPATA5 mutations cause a distinct autosomal recessive phenotype of intellectual disability, hypotonia and hearing loss. Orphanet J Rare Dis.
Chicago ZitierstilBuchert, Rebecca, et al. "SPATA5 Mutations Cause a Distinct Autosomal Recessive Phenotype of Intellectual Disability, Hypotonia and Hearing Loss." Orphanet J Rare Dis 2016.
MLA ZitierstilBuchert, Rebecca, et al. "SPATA5 Mutations Cause a Distinct Autosomal Recessive Phenotype of Intellectual Disability, Hypotonia and Hearing Loss." Orphanet J Rare Dis 2016.
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