학술논문 – 부산대학교 도서관

학술논문

replay검색결과 돌아가기

search검색화면

Mutations in PTPN11 could lead to a congenital myasthenic syndrome phenotype: a Noonan syndrome case series

Document Type

Article

Author

Pugliese, A.; Roos, A.; Thompson, R.; Polavarapu, K.; Lochmüller, H.; Della Marina, A.; Schara-Schmidt, U.; de Paula Estephan, E.; Zanoteli, E.; Hentschel, A.; Azuma, Y.; Töpf, A.

Source

In: Journal of Neurology. (Journal of Neurology, March 2024, 271(3):1331-1341)

Subject

Language

English

ISSN

14321459
03405354

Online Access

Full Text (ECC - 개별구독 전자저널) Web of Science JCR 저널정보 Scopus Find it@PNU

이메일