학술논문 – 부산대학교 도서관

학술논문

replay검색결과 돌아가기

search검색화면

Distinct novel mutations affecting the same base in the NIPA1 gene cause autosomal dominant hereditary spastic paraplegia in two Chinese families

Document Type

Journal

Author

Chen, SQ; Song, C; Guo, H; Xu, PY; Huang, WJ; Zhou, Y; Sun, JD; Li, CX; Du, Y; Li, XH; Liu, ZL; Geng, DQ; Maxwell, PH; Zhang, C; Wang, Y

Source

HUMAN MUTATION; 2005, 25 2, p135-p141, 7p.

Subject

Language

English

ISSN

10981004

Online Access

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

이메일