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Progetto Mitofusina2 - Le mutazioni del gene mitocondriale MFN2, che codifica la proteina Mitofusina2 sono causa della malattia CMT2A, la forma sensitvo-motoria assonale della CMT.La sigla CMT indica la sindrome di Charcot-Marie-Tooth, una malattia rara che comporta il disordine

Progetto Mitofusina2

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