Journal Articles
Intractable & Rare Diseases Research
Year : 2022
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https://amu.hal.science/hal-04035192
Submitted on : Friday, March 17, 2023-5:47:55 PM
Last modification on : Saturday, March 18, 2023-3:38:27 AM
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Ninon Fournier, Alexandre Fabre. Smooth muscle motility disorder phenotypes: A systematic review of cases associated with seven pathogenic genes (ACTG2, MYH11, FLNA, MYLK, RAD21, MYL9 and LMOD1). Intractable & Rare Diseases Research, 2022, 11 (3), pp.113-119. ⟨10.5582/irdr.2022.01060⟩. ⟨hal-04035192⟩
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