Publications
Export 3 results:
Author Title [ Year
] Filters: Author is Leal, Suzanne M and Keyword is Lod Score [Clear All Filters]
Autosomal-Recessive Hearing Impairment Due to Rare Missense Variants within S1PR2. Am J Hum Genet 98, 331-8 (2016).
COPA mutations impair ER-Golgi transport and cause hereditary autoimmune-mediated lung disease and arthritis. Nat Genet 47, 654-60 (2015).
