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Disrupted nitric oxide signaling due to GUCY1A3 mutations increases risk for moyamoya disease, achalasia and hypertension

Document Type

Article

Author

Wallace, S.; Guo, D.-C.; Regalado, E.; Mellor-Crummey, L.; Martin, E.; Berka, V.; Sharina, I.; Milewicz, D.M.; Bamshad, M.; Nickerson, D.A.; Dauser, R.; Hanchard, N.; Marom, R.; Ganesan, V.; Saunders, D.; Morris, S.A.

Source

In: Clinical Genetics. (Clinical Genetics, 1 October 2016, 90(4):351-360)

Subject

Language

English

ISSN

13990004
00099163

Online Access

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

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