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A founder mutation in Vps37A causes autosomal recessive complex hereditary spastic paraparesis

Document Type

Article

Author

Zivony-Elboum, Y.; Kfir, N.; Shoval, Y.; Khayat, M.; Falik-Zaccai, T.C.; Westbroek, W.; Savitzki, D.; Bloom, A.; Rod, R.; Gross, B.; Samri, W.; Cohen, H.; Sonkin, V.; Freidman, T.; Geiger, D.; Fattal-Valevski, A.; Anikster, Y.; Waters, A.M.; Kleta, R.

Source

In: Journal of Medical Genetics. (Journal of Medical Genetics, July 2012, 49(7):462-472)

Subject

Language

English

ISSN

00222593
14686244

Online Access

Full Text (BMJ Journals) Full Text (ProQuest Central) Web of Science JCR 저널정보 Scopus Find it@PNU

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