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HARVARD Citation
Abbasi‐Moheb, L. et al. (2021). Biallelic loss‐of‐function HACD1 variants are a bona fide cause of congenital myopathy. Clinical genetics. 99 (4), pp. 513-518. [Online].
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Abbasi‐Moheb, L. et al. (2021). Biallelic loss‐of‐function HACD1 variants are a bona fide cause of congenital myopathy. Clinical genetics. 99 (4), pp. 513-518. [Online].