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Case report: Unusual episodic myopathy in a patient with novel homozygous deletion of first coding exon of MICU1 gene https://t.co/ce2BeEUXxn
Case report: Unusual episodic myopathy in a patient with novel homozygous deletion of first coding exon of MICU1 gene https://t.co/ce2BeEUXxn
Case report: Unusual episodic myopathy in a patient with novel homozygous deletion of first coding exon of MICU1 gene https://t.co/NnEGUaAyQS https://t.co/YKuqE3c7Ob
New Research: Case report: Unusual episodic myopathy in a patient with novel homozygous deletion of first coding exon of MICU1 gene: We present a patient with unusual episodes of muscular weakness due to homozygous deletion of exon 2 in the… https://t.co/E