A new SLC20A2 mutation identified in southern Italy family with primary familial brain calcification-Reference-Cited by-同舟云学术

A new SLC20A2 mutation identified in southern Italy family with primary familial brain calcification

Published:2015-08 Issue:1 Volume:568 Page:109-111
ISSN:0378-1119
Container-title:Gene
language:en
Short-container-title:Gene

Author:

Gagliardi Monica,Morelli Maurizio,Annesi Grazia,Nicoletti Giuseppe,Perrotta Paolo,Pustorino Giuseppe,Iannello Grazia,Tarantino Patrizia,Gambardella Antonio,Quattrone Aldo

Publisher

Elsevier BV

Subject

Genetics,General Medicine

Reference22 articles.

1. SLC20A2 and THAP1 deletion in familial basal ganglia calcification with dystonia;Baker;Neurogenetics,2013

2. Fahr's disease linked to a novel SLC20A2 gene mutation manifesting with dynamic aphasia;Brighina;Neurodegener Dis,2014

3. Phenotypic heterogeneity of movement disorders due to intracranial calcifications with or without SLC20A2 mutations;Carecchio;Mov. Disord.,2014

4. Novel SLC20A2 mutations identified in southern Chinese patients with idiopathic basal ganglia calcification;Chen;Gene,2013

5. Idiopathische Verkalkung der Hirngefasse;Fahr;Zentralbl. Allg. Pathol. Anat.,1930

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