A Case of Manifesting Carrier with DMD Phenotype Cited by

Acta Medica > Archive > 2009, Vol. 52 > Issue 4 > p. 167 > Cited by

Acta Med. 2009, 52: 167-170

https://doi.org/10.14712/18059694.2016.125

Akshay Anand, Monika Vinish, Sudesh Prabhakar

Departments of Neurology, Postgraduate Institute of Medical Education and Research (PGIMER), Sector-12, Chandigarh, India

Received March 15, 2009
Accepted October 23, 2009

Tang Jin, Song Xueqin, Ji Guang, Wu Hongran, Sun Shuyan, Lu Shan, Li Yuan, Zhang Chi, Zhang Huiqing: A novel DMD splicing mutation found in a family responsible for X-linked dilated cardiomyopathy with hyper-CKemia. Medicine 2018, 97, e11074. <https://doi.org/10.1097/MD.0000000000011074>
Finsterer Josef, Stöllberger Claudia, Vlckova Zoja, Gencik Martin: On the edge of noncompaction: Minimally manifesting Duchenne carrier due to the dystrophin mutation n.2867A>C. International Journal of Cardiology 2013, 165, e18. <https://doi.org/10.1016/j.ijcard.2012.10.075>