Publication: Homozygous CAPN1 mutations causing a spastic-ataxia phenotype in 2 families
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Organization Authors
Co-Authors
Koçoğlu, Cemile
Gündoğdu, Aslı
Kocaman, Gülşen
Kahraman-Koytak, Pınar
Uluç, Kayıhan
Kızıltan, Güneş
Çağlayan, Ahmet Okay
Bilguv, Kaya
Başak, A. Nazli
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NO
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Lippincott Williams and Wilkins (LWW)
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Source
Neurology: Genetics
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DOI
10.1212/NXG.0000000000000218
