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Autosomal dominant spinal muscular atrophy with lower extremity predominance: A recognizable phenotype of BICD2 mutations
Rudnik-Schöneborn, Sabine, Deden, Florian, Eggermann, Katja, Eggermann, Thomas, Wieczorek, Dagmar, Sellhaus, Bernd, Yamoah, Alfred, Goswami, Anand, Claeys, Kristl G., Weis, Joachim, Zerres, KlausLanguage:
english
Journal:
Muscle & Nerve
DOI:
10.1002/mus.25114
Date:
July, 2016
File:
PDF, 2.51 MB
english, 2016