Soler-Palacín, P., Garcia Prat, M., Martín-Nalda, A., Franco-Jarava, C., Rivière, J. G., Plaja, A., . . . Colobran, R. (2018). LRBA deficiency in a patient with a novel homozygous mutation due to chromosome 4 segmental uniparental isodisomy.
Citación estilo ChicagoSoler-Palacín, Pere, et al. LRBA Deficiency in a Patient With a Novel Homozygous Mutation Due to Chromosome 4 Segmental Uniparental Isodisomy. 2018.
Cita MLASoler-Palacín, Pere, et al. LRBA Deficiency in a Patient With a Novel Homozygous Mutation Due to Chromosome 4 Segmental Uniparental Isodisomy. 2018.
Precaución: Estas citas no son 100% exactas.