Publications by authors named "Erin C Loring"

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Dominant De Novo Mutations in GJA1 Cause Erythrokeratodermia Variabilis et Progressiva, without Features of Oculodentodigital Dysplasia.
Lynn M Boyden, Brittany G Craiglow, Jing Zhou, Ronghua Hu, Erin C Loring

J Invest Dermatol· June 2015

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Somatic HRAS p.G12S mutation causes woolly hair and epidermal nevi.
Jonathan L Levinsohn, Joyce Teng, Brittany G Craiglow, Erin C Loring, T Andrew Burrow

J Invest Dermatol· April 2014

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Multilineage somatic activating mutations in HRAS and NRAS cause mosaic cutaneous and skeletal lesions, elevated FGF23 and hypophosphatemia.
Young H Lim, Diana Ovejero, Jeffrey S Sugarman, Cynthia M C Deklotz, Ann Maruri, Erin C Loring

Hum Mol Genet· January 2014

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