Associated Papers
The ATP Synthase Deficiency in Human Diseases.
Galber C et al.
Life (basel, Switzerland), 2021
Recent advances in the genetics of dystonia.
Xiao J et al.
Current Neurology and Neuroscience Reports, 2014
Genetic and allelic heterogeneity of Cryg mutations in eight distinct forms of dominant cataract in the mouse.
Graw J et al.
Investigative Ophthalmology & Visual Science, 2004
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