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Autosomal recessive mutations of GPR126 are responsible for severe Arthrogryposis multiplex congenita

Document Type

Journal

Author

Ravenscroft, G.; Nolen, F.; Rajagopalan, S.; Meireles, A.; Paavola, K.; Gaillard, D.; Alanio, E.; Buckland, M.; Arbuckle, S.; Krivanek, M.; Maluenda, J.; Pannell, S.; Gooding, R.; Ong, R.; Allcock, R.; Kok, F.; Talbot, W.; Melki, J.; Laing, N.

Source

NEUROMUSCULAR DISORDERS; OCT 2015, 25 pS186-pS186, 1p. Supplement: 2

Subject

Language

English

ISSN

18732364

Online Access

Full Text (ScienceDirect 종량제) Full Text (Clinical Key) Web of Science JCR 저널정보 Scopus Find it@PNU

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