AGXT Gene Mutations and Prevalence of Primary Hyperoxaluria Type 1 in Moroccan Population-Reference-Cited by-同舟云学术

AGXT Gene Mutations and Prevalence of Primary Hyperoxaluria Type 1 in Moroccan Population

Published:2015-11 Issue:11 Volume:19 Page:623-628
ISSN:1945-0265
Container-title:Genetic Testing and Molecular Biomarkers
language:en
Short-container-title:Genetic Testing and Molecular Biomarkers

Author:

Boualla Lamiae¹²,Tajir Mariam²³,Oulahiane Najat⁴,Lyahyai Jaber¹²,Laarabi Fatima Zahra²,Chafai Elalaoui Siham¹²,Soulami Kenza⁵,Ait Ouamar Hassan⁴,Sefiani Abdelaziz¹²

Affiliation:

1. Centre de Génomique Humaine, Faculté de Médecine et de Pharmacie, Université Mohammed V, Rabat, Maroc.

2. Département de Génétique Médicale, Institut National d'Hygiène, Rabat, Maroc.

3. Service de Génétique, CHU Mohammed VI, Marrakech, Maroc.

4. Service Pédiatrie IV, Hôpital d'Enfant, CHU Ibn Sina, Rabat, Maroc.

5. Cabinet of pediatric Nephrology, Casablanca, Maroc.

Publisher

Mary Ann Liebert Inc

Subject

Genetics(clinical),General Medicine

Link

http://www.liebertpub.com/doi/pdf/10.1089/gtmb.2015.0136

Reference26 articles.

1. End-stage renal disease in Kuwaiti children: An 8-year experience

2. Diagnostic biochimique et moléculaire de l’hyperoxalurie primaire de type 1 : étude tunisienne à propos de 15 cas

3. Epidemiology of primary hyperoxaluria type 1

4. Hyperoxalurie primitive

5. Primary Hyperoxaluria

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