Autosomal recessive mutations of GPR126 are responsible for severe arthrogryposis multiplex congenita (2015)
- Authors:
- Autor USP: KOK, FERNANDO - FM
- Unidade: FM
- DOI: 10.1016/j.nmd.2015.06.013
- Subjects: MOVIMENTO FETAL; MALFORMAÇÕES; ANORMALIDADES MUSCULOSQUELÉTICAS; ARTROPATIAS
- Language: Inglês
- Imprenta:
- Source:
- Título: Neuromuscular Disorders
- ISSN: 0960-8966
- Volume/Número/Paginação/Ano: v. 25, suppl. 2, p. S186, res. G.O.4, 2015
- Conference titles: International Congress of the World Muscle Society
- Este periódico é de acesso aberto
- Este artigo NÃO é de acesso aberto
-
ABNT
RAVENSCROFT, G. et al. Autosomal recessive mutations of GPR126 are responsible for severe arthrogryposis multiplex congenita. Neuromuscular Disorders. London: Faculdade de Medicina, Universidade de São Paulo. Disponível em: https://doi.org/10.1016/j.nmd.2015.06.013. Acesso em: 24 fev. 2026. , 2015 -
APA
Ravenscroft, G., Nolent, F., Rajagopalan, S., Meireles, A., Paavola, K., Gaillard, D., et al. (2015). Autosomal recessive mutations of GPR126 are responsible for severe arthrogryposis multiplex congenita. Neuromuscular Disorders. London: Faculdade de Medicina, Universidade de São Paulo. doi:10.1016/j.nmd.2015.06.013 -
NLM
Ravenscroft G, Nolent 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. Autosomal recessive mutations of GPR126 are responsible for severe arthrogryposis multiplex congenita [Internet]. Neuromuscular Disorders. 2015 ; 25 S186.[citado 2026 fev. 24 ] Available from: https://doi.org/10.1016/j.nmd.2015.06.013 -
Vancouver
Ravenscroft G, Nolent 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. Autosomal recessive mutations of GPR126 are responsible for severe arthrogryposis multiplex congenita [Internet]. Neuromuscular Disorders. 2015 ; 25 S186.[citado 2026 fev. 24 ] Available from: https://doi.org/10.1016/j.nmd.2015.06.013 - Clinical presentation of a complex neurodevelopmental disorder caused by mutations in ADNP
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Informações sobre o DOI: 10.1016/j.nmd.2015.06.013 (Fonte: oaDOI API)
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