Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia-Reference-Cited by-同舟云学术

Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia

Published:2016-05 Issue:5 Volume:98 Page:1038-1046
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Gan-Or Ziv,Bouslam Naima,Birouk Nazha,Lissouba Alexandra,Chambers Daniel B.,Vérièpe Julie,Androschuk Alaura,Laurent Sandra B.,Rochefort Daniel,Spiegelman Dan,Dionne-Laporte Alexandre,Szuto Anna,Liao Meijiang,Figlewicz Denise A.,Bouhouche Ahmed,Benomar Ali,Yahyaoui Mohamed,Ouazzani Reda,Yoon Grace,Dupré Nicolas,Suchowersky Oksana,Bolduc Francois V.,Parker J. Alex,Dion Patrick A.,Drapeau Pierre,Rouleau Guy A.,Ouled Amar Bencheikh Bouchra

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference44 articles.

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5. The extent of axonal loss in the long tracts in hereditary spastic paraplegia;Deluca;Neuropathol. Appl. Neurobiol.,2004

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