Concepedia

Publication | Open Access

KIF1A variants are a frequent cause of autosomal dominant hereditary spastic paraplegia

DOIFull Paper Access

91

Citations

27

References

2019

Year

Maartje Pennings, Meyke Schouten, Judith van Gaalen, Rowdy Meijer, Susanne T. de Bot, Marjolein Kriek, Christiaan G. J. Saris, Leonard H. van den Berg, Michael A. van Es, Dick M. H. Zuidgeest,
European Journal of Human Genetics

References

YearCitations

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