Comment on "Defining the Genetic Landscape of Congenital Mirror Movements in 80 Affected Individuals"

Oriane Trouillard^{1

2}, Aurélie Méneret^{2

3}, Margaux Dunoyer⁴, Mohamed Doulazmi⁵, Isabelle Dusart¹, Caroline Dubacq¹, Emmanuel Roze^{2

3}

Affiliations

¹ Sorbonne Université, INSERM, CNRS, Institut de Biologie Paris Seine, IBPS, Neuroscience Paris Seine, NPS, Paris, France.
² Sorbonne Université, Institut du Cerveau-Paris Brain Institute-ICM, Inserm, CNRS, AP-HP, Hôpital Pitié-Salpêtrière, Paris, France.
³ AP-HP, Hôpital Pitié-Salpêtrière, DMU Neuroscience 6, Paris, France.
⁴ Département de Neurologie, AP-HP, Hôpital Pitié-Salpêtrière, Paris, France.
⁵ Sorbonne Université, INSERM, CNRS, Institut de Biologie Paris Seine, IBPS, Biological Adaptation and Ageing, B2A, Paris, France.

Comment

Oriane Trouillard et al. Mov Disord. 2024 May.

. 2024 May;39(5):925-926.

doi: 10.1002/mds.29799.

Oriane Trouillard^{1

2}, Aurélie Méneret^{2

3}, Margaux Dunoyer⁴, Mohamed Doulazmi⁵, Isabelle Dusart¹, Caroline Dubacq¹, Emmanuel Roze^{2

3}

¹ Sorbonne Université, INSERM, CNRS, Institut de Biologie Paris Seine, IBPS, Neuroscience Paris Seine, NPS, Paris, France.
² Sorbonne Université, Institut du Cerveau-Paris Brain Institute-ICM, Inserm, CNRS, AP-HP, Hôpital Pitié-Salpêtrière, Paris, France.
³ AP-HP, Hôpital Pitié-Salpêtrière, DMU Neuroscience 6, Paris, France.
⁴ Département de Neurologie, AP-HP, Hôpital Pitié-Salpêtrière, Paris, France.
⁵ Sorbonne Université, INSERM, CNRS, Institut de Biologie Paris Seine, IBPS, Biological Adaptation and Ageing, B2A, Paris, France.

No abstract available

References

1. Collins Hutchinson ML, St‐Onge J, Schlienger S, et al. Defining the genetic landscape of congenital Mirror movements in 80 affected individuals. Mov Disord 2024;39(2):400–410. https://doi.org/10.1002/mds.29669
1. Richards S, Aziz N, Bale S, et al. Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology. Genet Med 2015;17(5):405–424.
1. Trouillard O, Dupaigne P, Dunoyer M, et al. Congenital mirror movements are associated with defective polymerisation of RAD51. J Med Genet 2023;60(11):1116–1126.
1. Meneret A, Franz EA, Trouillard O, et al. Mutations in the netrin‐1 gene cause congenital mirror movements. J Clin Invest 2017;127(11):3923–3936.
1. Schlienger S, Yam PT, Balekoglu N, et al. Genetics of mirror movements identifies a multifunctional complex required for Netrin‐1 guidance and lateralization of motor control. Sci Adv 2023;9(19):eadd5501.