De España a Bélgica: Hablando del síndrome CTNNB1 con Ana Gonzalez Hernández

Ana Gonzalez Hernández es la Vicepresidenta de la Fundación CTNNB1 y madre de una niña afectada por esta enfermedad. Ana nos cuenta su historia, desde la odisea de diagnóstico hasta como llego a ser vice presidenta de esta asociación. Desde su punto de vista como bióloga, madre, e hispana, ella nos habla de del síndrome CTNNB1 y de su fundación. https://ctnnb1-foundation.org/ Show Notes: Subscribe: Mas Que Raras Podcast Connect with BloodStream Media: BloodStreamMedia.com BloodStream on Facebook BloodStream on Twitter

Episode metadata supplied by the publisher feed · Published Sep 13, 2023

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De España a Bélgica: Hablando del síndrome CTNNB1 con Ana Gonzalez Hernández

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