Published in
Lippincott, Williams & Wilkins, Neurology: Genetics, 1(4), p. e218, 2018
DOI: 10.1212/nxg.0000000000000218
Links
Tools
Homozygous CAPN1 mutations causing a spastic-ataxia phenotype in 2 families
Journal article published in 2018 by
Cemile Kocoglu 
,
Asli Gundogdu,
Gulsen Kocaman,
Pinar Kahraman-Koytak,
Kayihan Uluc,
Gunes Kiziltan,
Ahmet Okay Caglayan,
Kaya Bilguvar,
Atay Vural,
A. Nazli Basak
,
Asli Gundogdu,
Gulsen Kocaman,
Pinar Kahraman-Koytak,
Kayihan Uluc,
Gunes Kiziltan,
Ahmet Okay Caglayan,
Kaya Bilguvar,
Atay Vural,
A. Nazli Basak
This paper is made freely available by the publisher.
Full text: Download
Data provided by 