Work

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

Year: 2015

Type: article

Source: Neuromuscular Disorders

DOI: 10.1016/j.nmd.2015.06.013

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

Institutions: Harry Perkins Institute of Medical Research, Université Paris-Sud, Liverpool Hospital, Stanford University, Children's Hospital at Westmead, Pathwest Laboratory Medicine, The University of Western Australia, Universidade de São Paulo

Language: English

Topic: Congenital limb and hand anomalies

Subfield: Developmental Biology

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

OpenAlex ID: W2176736734

FWCI:

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