학술논문 – 부산대학교 도서관

학술논문

replay검색결과 돌아가기

search검색화면

Homozygosity for frameshift mutations in XYLT2 result in a spondylo-ocular syndrome with bone fragility, cataracts, and hearing defects

Document Type

Article

Author

Munns, C.F.; Biggin, A.; Fahiminiya, S.; Majewski, J.; Poudel, N.; Munteanu, M.C.; Hinsdale, M.E.; Sillence, D.O.; Metcalf, J.P.; Glorieux, F.; Fassier, F.; Rauch, F.

Source

In: American Journal of Human Genetics. (American Journal of Human Genetics, 4 June 2015, 96(6):971-978)

Subject

Language

English

ISSN

15376605
00029297

Online Access

Full Text (ScienceDirect 종량제) Full Text (ScienceDirect O/A) Open Access (EBSCO) Web of Science JCR 저널정보 Scopus Find it@PNU

이메일