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

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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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Lippincott Williams and Wilkins (LWW)

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Clinical neurology

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Neurology: Genetics

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10.1212/NXG.0000000000000218

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