Novel compound heterozygous mutations of LAMA2-limb–girdle muscular dystrophy: A case report and literature review

Overview of attention for article published in Frontiers in Neurology, February 2023

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RT @DrImranSheikh: Novel compound heterozygous mutations of LAMA2-limb–girdle muscular dystrophy: A case report and literature review https…

16 Feb 2023

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Novel compound heterozygous mutations of LAMA2-limb–girdle muscular dystrophy: A case report and literature review https://t.co/UTBJfUTglQ https://t.co/8uxxGrkzh2

16 Feb 2023

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New Research: Novel compound heterozygous mutations of LAMA2-limb–girdle muscular dystrophy: A case report and literature review: The laminin α2 (LAMA2) gene pathogenic variants can lead to limb–girdle muscular dystrophy (known as LGMDR23),… https://t.co/j

13 Feb 2023

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