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APA Citation
Willis, T., Wood, C., Hudson, J., Polvikoski, T., Barresi, R., Lochmüller, H., Bushby, K., & Straub, V. (2016). muscle hypertrophy as the presenting sign in a patient with a complete FHL1 deletion. Clinical genetics, 90(2), 166–170. http://access.bl.uk/ark:/81055/vdc_100034809914.0x00004e