Homozygous CAPN1 mutations causing a spastic-ataxia phenotype in 2 families

Date
2018
Author
Bilguv, Kaya
Kocoglu, Cemile
Gundogdu, Asli
KAHRAMAN KOYTAK, PINAR
ULUÇ, KAYIHAN
Caglayan, Ahmet Okay
Kocaman, Gulsen
Kiziltan, Gunes
Basak, A. Nazli
Vural, Atay
Metadata
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URI
http://hdl.handle.net/20.500.12627/132395
https://doi.org/10.1212/nxg.0000000000000218
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