A novel phenotype of AChR-deficiency syndrome with predominant facial and distal weakness resulting from the inclusion of an evolutionary alternatively-spliced exon in CHRNA1

MLA

Pedro M Rodríguez Cruz, et al. “A Novel Phenotype of AChR-Deficiency Syndrome with Predominant Facial and Distal Weakness Resulting from the Inclusion of an Evolutionary Alternatively-Spliced Exon in CHRNA1.” Neuromuscular Disorders, vol. 33, Feb. 2023, pp. 161–68. EBSCOhost, https://doi.org/10.1016/j.nmd.2022.12.011.

APA

Pedro M Rodríguez Cruz, Gianina Ravenscroft, Daniel Natera, Aisling Carr, Adnan Manzur, Wei Wei Liu, Norbert R Vella, Ivonne Jericó, Lidia Gonzalez-Quereda, Pia Gallano, Simon Attard Montalto, Mark R Davis, Phillipa J Lamont, Nigel G Laing, Pierre Bourque, Andres Nascimento, Francesco Muntoni, Kiran Polavarapu, Hanns Lochmüller, … David Beeson. (2023). A novel phenotype of AChR-deficiency syndrome with predominant facial and distal weakness resulting from the inclusion of an evolutionary alternatively-spliced exon in CHRNA1. Neuromuscular Disorders, 33, 161–168. https://doi.org/10.1016/j.nmd.2022.12.011

Chicago

Pedro M Rodríguez Cruz, Gianina Ravenscroft, Daniel Natera, Aisling Carr, Adnan Manzur, Wei Wei Liu, Norbert R Vella, et al. 2023. “A Novel Phenotype of AChR-Deficiency Syndrome with Predominant Facial and Distal Weakness Resulting from the Inclusion of an Evolutionary Alternatively-Spliced Exon in CHRNA1.” Neuromuscular Disorders 33 (February): 161–68. doi:10.1016/j.nmd.2022.12.011.