Mura-Escorche, G.; García-Suarez, L.C.; Lebredo-Álvarez, I.; Ramos-Trujillo, E.; Claverie-Martin, F.
Identification of a Novel Homozygous SLC34A1 Missense Mutation and a Heterozygous SLC34A3 Deletion in an Infant with Nephrocalcinosis, Failure to Thrive, and Hypercalcemia. Int. J. Mol. Sci. 2025, 26, 8541.
https://doi.org/10.3390/ijms26178541
AMA Style
Mura-Escorche G, García-Suarez LC, Lebredo-Álvarez I, Ramos-Trujillo E, Claverie-Martin F.
Identification of a Novel Homozygous SLC34A1 Missense Mutation and a Heterozygous SLC34A3 Deletion in an Infant with Nephrocalcinosis, Failure to Thrive, and Hypercalcemia. International Journal of Molecular Sciences. 2025; 26(17):8541.
https://doi.org/10.3390/ijms26178541
Chicago/Turabian Style
Mura-Escorche, Glorián, Leire C. García-Suarez, Isis Lebredo-Álvarez, Elena Ramos-Trujillo, and Felix Claverie-Martin.
2025. "Identification of a Novel Homozygous SLC34A1 Missense Mutation and a Heterozygous SLC34A3 Deletion in an Infant with Nephrocalcinosis, Failure to Thrive, and Hypercalcemia" International Journal of Molecular Sciences 26, no. 17: 8541.
https://doi.org/10.3390/ijms26178541
APA Style
Mura-Escorche, G., García-Suarez, L. C., Lebredo-Álvarez, I., Ramos-Trujillo, E., & Claverie-Martin, F.
(2025). Identification of a Novel Homozygous SLC34A1 Missense Mutation and a Heterozygous SLC34A3 Deletion in an Infant with Nephrocalcinosis, Failure to Thrive, and Hypercalcemia. International Journal of Molecular Sciences, 26(17), 8541.
https://doi.org/10.3390/ijms26178541