Publications
Export 1 results:
Author Title [ Year
] Filters: Author is Schoch, Kelly and Keyword is Genome-Wide Association Study [Clear All Filters]
A Recurrent De Novo Variant in NACC1 Causes a Syndrome Characterized by Infantile Epilepsy, Cataracts, and Profound Developmental Delay. Am J Hum Genet 100, 343-351 (2017).
