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Paper Details

Homozygous <i>CAPN1</i> mutations causing a spastic-ataxia phenotype in 2 families.
Neurol Genet
18
2018
Author NameAffiliation
Ahmet Okay CaglayanSuna and Inan Kirac Foundation (C.K., Bogazici University, Bezmialem Vakif University, Marmara University, Istanbul University, Istanbul Bilim University, Yale University School of Medicine, Yale Center for Genome Analysis, Koc University Hospital
Kaya BilguvarSuna and Inan Kirac Foundation (C.K., Bogazici University, Bezmialem Vakif University, Marmara University, Istanbul University, Istanbul Bilim University, Yale University School of Medicine, Yale Center for Genome Analysis, Koc University Hospital
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