Distinct Clinical and Genetic Findings in Iranian Patients With Glycogen Storage Disease Type 3-Reference-Cited by-同舟云学术

Distinct Clinical and Genetic Findings in Iranian Patients With Glycogen Storage Disease Type 3

Published:2018-06 Issue:4 Volume:19 Page:203-210
ISSN:1522-0443
Container-title:Journal of Clinical Neuromuscular Disease
language:en
Short-container-title:

Author:

Nazari Ferdos,Sinaei Farnaz,Nilipour Yalda,Petit François,Oveisgharan Shahram,Nassiri-Toosi Mohsen,Razzaghy-Azar Maryam,Mahmoudi Mahdi,Nafissi Shahriar

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical),Neurology,General Medicine

Reference20 articles.

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2. Glycogen storage disease type III: diagnosis, genotype, management, clinical course and outcome;Sentner;J Inherit Metab Dis.,2016

3. A novel nonsense mutation of the AGL gene in a Romanian patient with glycogen storage disease type IIIa;Zimmermann;Case Rep Genet.,2016

4. Glycogen storage disease type III in Egyptian children: a single centre clinico-laboratory study;El-Karaksy;Arab J Gastroenterol.,2014

5. A method and server for predicting damaging missense mutations;Adzhubei;Nat Methods,2010

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