학술논문 – 부산대학교 도서관

학술논문

replay검색결과 돌아가기

search검색화면

Biallelic variants in COPB1 cause a novel, severe intellectual disability syndrome with cataracts and variable microcephaly

Document Type

Article

Author

Macken, W.L.; Douglas, A.G.L.; Baralle, D.; Godwin, A.; Guille, M.; Wheway, G.; Nazlamova, L.; Wai, H.A.; Self, J.; Stals, K.; Ellard, S.; Alfares, A.; Aloraini, T.; AlSubaie, L.; Alfadhel, M.; Alajaji, S.; Kao, A.P.

Source

In: Genome Medicine. (Genome Medicine, December 2021, 13(1))

Subject

Language

English

ISSN

1756994X

Online Access

EBSCOHost PDF Full Text (Gale Academic Onefile) Full Text (ProQuest Central) Open Access (BioMed Central) Web of Science JCR 저널정보 Scopus Find it@PNU

이메일