MRPL44 mutations cause a slowly progressive multisystem disease with childhood-onset hypertrophic cardiomyopathy

Overview of attention for article published in neurogenetics, March 2015

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Mitochondrial MRPL44 mutation may be extremely rare cause of hemiplegic #migraine. Case report. http://t.co/Y1Yv5IAF2F

Mitochondrial MRPL44 mutation may be extremely rare cause of hemiplegic #migraine. Case report. http://t.co/Y1Yv5IAF2F

Mitochondrial MRPL44 mutation may be extremely rare cause of hemiplegic #migraine. Case report. http://t.co/Y1Yv5IAF2F

Mitochondrial MRPL44 mutation may be extremely rare cause of hemiplegic #migraine. Case report. http://t.co/Y1Yv5IAF2F

MRPL44 mutations cause a slowly progressive multisystem disease with childhood-onset hypertrophic cardiomyopathy http://t.co/GO9uhzh1vK

Pubmed: MRPL44 mutations cause a slowly progressive multisystem disease with childhood-onset hypertrophic… http://t.co/3JTXHEAcq3

MRPL44 mutations cause a slowly progressive multisystem disease with childhood-onset hypertrophic cardiomyopat... http://t.co/Ak6mxQ3z7P

#cardiology MRPL44 mutations cause a slowly progressive multisystem disease with childhood-onset hypert... http://t.co/LM8GjdRTyB #heart