A SLC20A2 gene mutation carrier displaying ataxia and increased levels of cerebrospinal fluid phosphate
Author:
Publisher
Elsevier BV
Subject
Clinical Neurology,Neurology
Reference12 articles.
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2. Update and mutational analysis of SLC20A2: a major cause of primary familial brain calcification;Lemos;Hum. Mutat.,2015
3. Evaluation of SLC20A2 mutations that cause idiopathic basal ganglia calcification in Japan;Yamada;Neurology,2014
4. Progressive brain calcifications and signs in a family with the L9R mutation in the PDGFB gene;Paucar;Neurol. Genet.,2016
5. Primary familial brain calcification;Sobrido,1993
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