| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 8806081 | International Journal of Pediatric Otorhinolaryngology | 2018 | 16 Pages |
Abstract
We identified two novel missense mutations p.Arg8Gly and p.Thr36Asn in exon 1 of BSND gene; both mutations were described for the first time in Moroccan patients with Bartter syndrome type IV.
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Authors
Soukaina Elrharchi, Zied Riahi, Sara Salime, Halima Nahili, Hassan Rouba, Mostafa Kabine, Crystel Bonnet, Christine Petit, Abdelhamid Barakat,