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VPS13D-based disease: Expansion of the clinical phenotype in two brothers and mutation diversity in the Turkish population

DOI Web Site Web Site 1 Citations

Journal

Revue Neurologique

Revue Neurologique 178 (9), 907-913, 2022-11

Elsevier BV

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Keywords

Details 詳細情報について

CRID

1360580931197708672
DOI

10.1016/j.neurol.2022.05.005
ISSN

00353787
Web Site

https://api.elsevier.com/content/article/PII:S0035378722007196?httpAccept=text/xml

https://api.elsevier.com/content/article/PII:S0035378722007196?httpAccept=text/plain
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