VP417 Obstetric and gynaecological features in females carrying mutations in the skeletal muscle ryanodine receptor (RYR1) gene: a questionnaire study

Neuromuscular Disorders - Tập 33 - Trang S128 - 2023
A. Mistry1, G. Saldanha1, L. van den Bersselaar2, S. Treves3, M. Goldberg4, N. Voermans5, R. Tribe1, H. Jungbluth6,7
1Dept Women and Children's Health, School of Life Course Sciences, Faculty of Life Sciences and Medicine, Kings College London, UK
2Malignant Hyperthermia Investigation Unit, Dept Anesthesiology, Canisius Wilhelmina Hospital, Nijmegen, NL
3Dept Biomedicine, Univ Hosp Basel, Switzerland
4RYR1 Foundation, Pittsburgh, USA
5Dept Neurology, Radboud Univ Med Centre, Nijmegen, NL
6Dept Paed Neurology, Neuromusc Service, Evelina Ch Hosp, Guy's & St Thomas’ NHS Foundation Trust, London, UK
7Randall Centre for Cell & Molecular Biophysics, Muscle Signalling Section, Fac Life Sciences & Medicine (FoLSM), King's College London, UK

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Neuromuscular Disorders

Tập 33

S128

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