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SLC35F1 as a candidate gene for neurodevelopmental disorders resembling Rett syndrome.
Elisabetta Di Fede
Angela Peron
Elisa Adele Colombo
Cristina Gervasini
Aglaia Vignoli
Published in:
American journal of medical genetics. Part A (2021)
Keyphrases
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genome wide
case report
genome wide identification
congenital heart disease