Xeroderma pigmentosum complementation group F: A rare cause of cerebellar ataxia with chorea
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),Neurology
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1. The autosomal recessive cerebellar ataxias;Anheim;N. Engl. J. Med.,2012
2. Mini-exome coupled to read-depth based copy number variation analysis in patients with inherited ataxias;Marelli;Hum. Mutat.,2016
3. Xeroderma pigmentosum;Lehmann;Orphanet J. Rare Dis.,2011
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5. Xeroderma pigmentosum complementation group F in a non-Japanese patient;Norris;J. Am. Acad. Dermatol.,1988
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