Genetic and clinical characterization of 73 Pigmentary Mosaicism patients: revealing the genetic basis of clinical manifestations.

Autor: Salas-Labadía, C.¹ (AUTHOR) consusa@hotmail.com, Gómez-Carmona, S.^2,3 (AUTHOR), Cruz-Alcívar, R.^1,4,5 (AUTHOR), Martínez-Anaya, D.¹ (AUTHOR), Del Castillo-Ruiz, V.³ (AUTHOR), Durán-McKinster, C.⁶ (AUTHOR), Ulloa-Avilés, V.¹ (AUTHOR), Yokoyama-Rebollar, E.³ (AUTHOR), Ruiz-Herrera, A.⁷ (AUTHOR), Navarrete-Meneses, P.¹ (AUTHOR), Lieberman-Hernández, E.³ (AUTHOR), González-Del Angel, A.⁸ (AUTHOR), Cervantes-Barragán, D.⁹ (AUTHOR), Villarroel-Cortés, C.³ (AUTHOR), Reyes-León, A.¹ (AUTHOR), Suárez-Pérez, D.³ (AUTHOR), Pedraza-Meléndez, A.^1,10 (AUTHOR), González-Orsuna, A.¹ (AUTHOR), Pérez-Vera, P.¹ (AUTHOR) pperezvera@yahoo.com

Publikováno v: Orphanet Journal of Rare Diseases. 11/15/2019, Vol. 14 Issue 1, p1-11. 11p.

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