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Autor:
Bouramtane, Abdelhamid, Moufid, Fatima Zohra, Ahakoud, Mohamed, Bouguenouch, Laila, Ouldim, Karim
Publikováno v:
In Genetics in Medicine Open 2023 1(1) Supplement
Autor:
Bouramtane, Abdelhamid, El Azami El Idrissi, Hajar, Ahakoud, Mohamed, Elmakhzen, Badreddine, Lazraq, Ahmed, Bouguenouch, Laila, Ouldim, Karim
Publikováno v:
In Genetics in Medicine Open 2023 1(1) Supplement
Autor:
Bouramtane, Abdelhamid, Moufid, Fatima Zahra, Ahakoud, Mohamed, Bouguenouch, Laila, Ouldim, Karim
Publikováno v:
In Genetics in Medicine Open 2023 1(1) Supplement
Publikováno v:
Cureus.
Nephrolithiasis (NL) and urolithiasis (UL) are usual reasons for hospitalization and presentation in pediatric outpatient departments and their incidence continues to rise worldwide. In Morocco, a previous epidemiological study done in the Fez region
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::31daefff31dd940c1e9fadc29877d315
https://doi.org/10.7759/cureus.23616
https://doi.org/10.7759/cureus.23616
Mutations in the NPHS2 gene encoding podocin are implicated in an autosomal-recessive form of nonsyndromic steroid-resistant nephrotic syndrome in both pediatric and adult patients. The p.R138Q (c.413G>A) mutation in exon 3 was the most prevalent mut
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2659::6be8e98a10d0d92dd386963d5e44b884
https://zenodo.org/record/5701799
https://zenodo.org/record/5701799
Autor:
Belghiti, Hanae Daha, Abbassi, Meriame, Sayel, Hanane, Ahakoud, Mohamed, El Makhzen, Badr Eddine, Lee, Norman, Russo, Silvia, Chaouki, Sana, Bouguenouch, Laila
Publikováno v:
Journal of Pediatric Genetics; 20240101, Issue: Preprints