Soler-Palacín, P., Garcia-Prat, M., Martín-Nalda, A., Franco-Jarava, C., Rivière, J. G., Plaja Rustein, A., . . . Colobrán Oriol, R. (2018). LRBA Deficiency in a Patient With a Novel Homozygous Mutation Due to Chromosome 4 Segmental Uniparental Isodisomy.
Citación estilo ChicagoSoler-Palacín, Pere|||0000-0002-0346-5570, et al. LRBA Deficiency in a Patient With a Novel Homozygous Mutation Due to Chromosome 4 Segmental Uniparental Isodisomy. 2018.
Cita MLASoler-Palacín, Pere|||0000-0002-0346-5570, et al. LRBA Deficiency in a Patient With a Novel Homozygous Mutation Due to Chromosome 4 Segmental Uniparental Isodisomy. 2018.
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