CLAPO syndrome: identification of somatic activating PIK3CA mutations and delineation of the natural history and phenotype
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P. Lapunzina | F. Santos-Simarro | K. Ibáñez | J. Nevado | R. Mena | J. López-Gutiérrez | E. Vallespín | C. Ayuso | Á. Del Pozo | A. Bustamante | S. García-Miñaúr | R. Martín-Arenas | V. Ruiz-Perez | V. Martínez-Glez | C. Villaverde | G. Gordo | L. Rodríguez-Laguna | Inmaculada Rueda-Arenas | Noelia Agra | Victoria E Fernández-Montaño | H. González-Pecellín | M. V. Gomez