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Rhnull phenotype caused by a novel RHAG mutation, c.945+1G>A, in the Japanese population

Document Type

Article

Author

Ushiki, T.; Kamimura, M.; Nakata, K.; Tsuneyama, H.; Uchikawa, M.; Masuko, M.; Katagiri, T.; Kozakai, T.; Kasami, T.; Tanaka, T.; Kitajima, T.; Kasai, E.; Komata, T.; Fuse, I.; Sato, K.; Ogasawara, K.

Source

In: Transfusion. (Transfusion, 2019, 59(8):2519-2522)

Subject

Language

English

ISSN

15372995
00411132

Online Access

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

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