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DST variants are responsible for neurogenic arthrogryposis multiplex congenita enlarging the spectrum of type VI hereditary sensory autonomic neuropathy

Document Type

Article

Author

Capri, Y.; Bourmance, L.; Melki, J.; Dupont, C.; Saint-Frison, M.-H.; Guimiot, F.; Grotto, S.; Chitrit, Y.; Laquerrière, A.

Source

In: Clinical Genetics. (Clinical Genetics, November 2023, 104(5):587-592)

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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