المؤلفون: Soledad Kleppe, James T. Lu, Phillipe M. Campeau, Abbhirami Rajagopal, Ignacio Bergadá, Brendan Lee, Florencia Clément, Richard A. Gibbs, Jose Miguel Liern, Debora Braslavsky, Hamilton Cassinelli, Graciela Vallejo, David S. Liu

المصدر: The Journal of Clinical Endocrinology & Metabolism. 99:E2451-E2456

مصطلحات موضوعية: Male, medicine.medical_specialty, Hypophosphatemia, Endocrinology, Diabetes and Metabolism, DNA Mutational Analysis, Hypercalciuria, Clinical Biochemistry, Context (language use), Biology, Sodium-Phosphate Cotransporter Proteins, Type IIa, Biochemistry, symbols.namesake, Endocrinology, Internal medicine, medicine, Humans, Exome, Child, Exome sequencing, Sanger sequencing, Genetics, JCEM Online: Advances in Genetics, Biochemistry (medical), medicine.disease, Pedigree, Nephrocalcinosis, Phenotype, Parathyroid Hormone, Child, Preschool, Mutation, Mutation (genetic algorithm), Hypercalcemia, symbols, Female

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e8546f2dca8c53ef8e6fc14e81ee2935
https://doi.org/10.1210/jc.2014-1517

المؤلفون: Jose Miguel, Liern, Vallejo, Graciela V.

المصدر: Pediatric Nephrology ; volume 22, issue 2, page 315-316 ; ISSN 0931-041X 1432-198X

الاتاحة: http://dx.doi.org/10.1007/s00467-006-0302-4
http://link.springer.com/content/pdf/10.1007/s00467-006-0302-4.pdf
http://link.springer.com/article/10.1007/s00467-006-0302-4/fulltext.html
http://link.springer.com/content/pdf/10.1007/s00467-006-0302-4