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Mutation in the PYK2-Binding Domain of PITPNM3 Causes Autosomal Dominant Cone Dystrophy (CORD5) in Two Swedish Families
Recent Advances in Retinal Degeneration
Advances in experimental medicine and biology, January 2008
Linda Köhn, Konstantin Kadzhaev, Marie S.I. Burstedt, Susann Haraldsson, Ola Sandgren, Irina Golovleva
The data shown below were compiled from readership statistics for 3 Mendeley readers of this research output. Click here to see the associated Mendeley record.
|Readers by professional status||Count||As %|
|Professor > Associate Professor||1||33%|
|Student > Master||1||33%|
|Readers by discipline||Count||As %|
|Medicine and Dentistry||2||67%|
|Biochemistry, Genetics and Molecular Biology||1||33%|