Smooth muscle motility disorder phenotypes: A systematic review of cases associated with seven pathogenic genes (<i>ACTG2</i>, <i>MYH11</i>, <i>FLNA</i>, <i>MYLK</i>, <i>RAD21</i>, <i>MYL9</i> and <i>LMOD1</i>) - Aix-Marseille Université Access content directly
Journal Articles Intractable & Rare Diseases Research Year : 2022

Smooth muscle motility disorder phenotypes: A systematic review of cases associated with seven pathogenic genes (ACTG2, MYH11, FLNA, MYLK, RAD21, MYL9 and LMOD1)

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hal-04035192 , version 1 (17-03-2023)

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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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