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Mutation spectrum of primary hyperoxaluria type 1 in Tunisia: Implication for diagnosis in North Africa

✍ Scribed by Nagara, Majdi; Tiar, Afaf; Ben Halim, Nizar; Ben Rhouma, Faten; Messaoud, Olfa; Bouyacoub, Yosra; Kefi, Rym; Hassayoun, Saida; Zouari, Noura; Ben Ammar, Mohamed Slim; Abdelhak, Sonia; Chemli, Jalel

Book ID: 120546171
Publisher: Elsevier Science
Year: 2013
Tongue: English
Weight: 254 KB
Volume: 527
Category: Article
ISSN: 0378-1119
DOI: 10.1016/j.gene.2013.06.023

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