Publications by authors named "Lamia Boualla"

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Associations between clinical characteristics and angiotensin-converting enzyme gene insertion/deletion polymorphism in Moroccan population with Type-2 diabetic nephropathy.
Maria Mansouri, Amal Zniber, Lamia Boualla, Ghizlane El Badaoui, Mariam Benkacem

Saudi J Kidney Dis Transpl· July 2019

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Correction to: Exome sequencing reveals a novel PLP1 mutation in a Moroccan family with connatal Pelizaeus-Merzbacher disease: a case report.
Jaber Lyahyai, Bouchra Ouled Amar Bencheikh, Siham C Elalaoui, Maria Mansouri, Lamia Boualla

BMC Pediatr· April 2018

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Exome sequencing reveals a novel PLP1 mutation in a Moroccan family with connatal Pelizaeus-Merzbacher disease: a case report.
Jaber Lyahyai, Bouchra Ouled Amar Bencheikh, Siham C Elalaoui, Maria Mansouri, Lamia Boualla

BMC Pediatr· February 2018

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