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Author/Creator Gal, Aniko

2. MSTO1 is a cytoplasmic pro‐mitochondrial fusion protein, whose mutation induces myopathy and ataxia in humans. Issue 7 (29th May 2017)

Authors:
Gal, Aniko; Balicza, Peter; Weaver, David; Naghdi, Shamim; Joseph, Suresh K; Várnai, Péter; Gyuris, Tibor; Horváth, Attila; Nagy, Laszlo; Seifert, Erin L; Molnar, Maria Judit; Hajnóczky, György
Journal:
EMBO molecular medicine
Issue:
Volume 9:Issue 7(2017)
Page Start:
967
Record Type:
Journal Article
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4. Recessive mutations in MSTO1 cause mitochondrial dynamics impairment, leading to myopathy and ataxia. Issue 8 (6th June 2017)

Authors:
Nasca, Alessia; Scotton, Chiara; Zaharieva, Irina; Neri, Marcella; Selvatici, Rita; Magnusson, Olafur Thor; Gal, Aniko; Weaver, David; Rossi, Rachele; Armaroli, Annarita; Pane, Marika; Phadke, Rahul; Sarkozy, Anna; Muntoni, Francesco; Hughes, Imelda; Cecconi, Antonella; Hajnóczky, György; Donati,...
Journal:
Human mutation
Issue:
Volume 38:Issue 8(2017)
Page Start:
970
Record Type:
Journal Article
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5. Retrospective assessment of the most common mitochondrial DNA mutations in a large Hungarian cohort of suspect mitochondrial cases. (August 2015)

Authors:
Remenyi, Viktoria; Inczedy-Farkas, Gabriella; Komlosi, Katalin; Horvath, Rita; Maasz, Anita; Janicsek, Ingrid; Pentelenyi, Klara; Gal, Aniko; Karcagi, Veronika; Melegh, Bela; Molnar, Maria Judit
Journal:
Mitochondrial DNA
Issue:
Volume 26:Number 4(2015:Aug.)
Page Start:
572
Record Type:
Journal Article
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