Report of a novel ATP7A mutation causing distal motor neuropathy-Reference-Cited by-同舟云学术

Report of a novel ATP7A mutation causing distal motor neuropathy

Published:2019-10 Issue:10 Volume:29 Page:776-785
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Gualandi Francesca,Sette Elisabetta,Fortunato Fernanda,Bigoni Stefania,De Grandis Domenico,Scotton Chiara,Selvatici Rita,Neri Marcella,Incensi Alex,Liguori Rocco,Storbeck Markus,Karakaya Mert,Simioni Valentina^ORCID,Squarzoni Stefano,Timmerman Vincent,Wirth Brunhilde,Donadio Vincenzo,Tugnoli Valeria,Ferlini Alessandra

Publisher

Elsevier BV

Subject

Genetics(clinical),Clinical Neurology,Neurology,Pediatrics, Perinatology, and Child Health

Reference29 articles.

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4. Occipital horn syndrome: report of a patient and review of the literature;Tsukahara;Clin Genet,1994

5. Translational research investigations on ATP7A: an important human copper ATPase;Kaler;Ann N Y Acad Sci,2014

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