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Loss-of-function variants in NFIA provide further support that NFIA is a critical gene in 1p32-p31 deletion syndrome: A four patient series.

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Description scientific article published on 22 September 2017
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author: John Pappas  Jane Juusola  Kwame Anyane-Yeboa  Anya Revah-Politi 

Publication date September 22, 2017
Language English
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