Cite
HARVARD Citation
Višnjar, T. et al. (2022). Biallelic ATOH1 Gene Variant in Siblings With Pontocerebellar Hypoplasia, Developmental Delay, and Hearing Loss. Neurology. p. . [Online].
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Višnjar, T. et al. (2022). Biallelic ATOH1 Gene Variant in Siblings With Pontocerebellar Hypoplasia, Developmental Delay, and Hearing Loss. Neurology. p. . [Online].