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Genetic study of SMA patients without homozygousSMN1deletions: identification of compound heterozygotes and characterisation of novel intragenicSMN1mutations

✍ Scribed by Yolanda Martín; Ana Valero; Emilia del Castillo; Samuel I. Pascual; Concepción Hernández-Chico

No coin nor oath required. For personal study only.

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