Cite
HARVARD Citation
Palmer, E. et al. (2021). CHEDDA syndrome is an underrecognized neurodevelopmental disorder with a highly restricted ATN1 mutation spectrum. Clinical genetics. 100 (4), pp. 468-477. [Online].
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Palmer, E. et al. (2021). CHEDDA syndrome is an underrecognized neurodevelopmental disorder with a highly restricted ATN1 mutation spectrum. Clinical genetics. 100 (4), pp. 468-477. [Online].