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

詳細情報 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

• データソース種別

  • Crossref