Publications
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Author Title [ Year
] Filters: Author is Lalani, Seema R and Keyword is Chromosomes, Human, Pair 5 [Clear All Filters]
Mutations in PURA cause profound neonatal hypotonia, seizures, and encephalopathy in 5q31.3 microdeletion syndrome. Am J Hum Genet 95, 579-83 (2014).
