Publications
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Author Title [ Year
] Filters: Author is Boyden, Lynn M and Keyword is Sequence Homology, Amino Acid [Clear All Filters]
Dominant De Novo Mutations in GJA1 Cause Erythrokeratodermia Variabilis et Progressiva, without Features of Oculodentodigital Dysplasia. J Invest Dermatol 135, 1540-1547 (2015).
