학술논문 – 부산대학교 도서관

학술논문

replay검색결과 돌아가기

search검색화면

Biallelic mutation in CHP1 causes human autosomal recessive ataxia by impairing NHE1 membrane targeting

Document Type

Journal

Author

Ferreira, N. Mendoza; Coutelier, M.; Janzen, E.; Hosseinibarkooie, S.; Lohr, H.; Schneider, S.; Milbradt, J.; Karakaya, M.; Riessland, M.; Pichlo, C.; Torres-Benito, L.; Singleton, A.; Zuchner, S.; Brice, A.; Durr, A.; Hammerschmidt, M.; Stevanin, G.; Wirth, B.

Source

EUROPEAN JOURNAL OF HUMAN GENETICS; JUL 2019, 27 p320-p321, 2p. Supplement: 1

Subject

Language

English

ISSN

14765438

Online Access

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

이메일