Rare Variants in MME , Encoding Metalloprotease Neprilysin, Are Linked to Late-Onset Autosomal-Dominant Axonal Polyneuropathies-Reference-Cited by-同舟云学术

Rare Variants in MME , Encoding Metalloprotease Neprilysin, Are Linked to Late-Onset Autosomal-Dominant Axonal Polyneuropathies

Published:2016-09 Issue:3 Volume:99 Page:607-623
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Auer-Grumbach Michaela,Toegel Stefan,Schabhüttl Maria,Weinmann Daniela,Chiari Catharina,Bennett David L.H.,Beetz Christian,Klein Dennis,Andersen Peter M.,Böhme Ilka,Fink-Puches Regina,Gonzalez Michael,Harms Matthew B.,Motley William,Reilly Mary M.,Renner Wilfried,Rudnik-Schöneborn Sabine,Schlotter-Weigel Beate,Themistocleous Andreas C.,Weishaupt Jochen H.,Ludolph Albert C.,Wieland Thomas,Tao Feifei,Abreu Lisa,Windhager Reinhard,Zitzelsberger Manuela,Strom Tim M.,Walther Thomas,Scherer Steven S.,Züchner Stephan,Martini Rudolf,Senderek Jan

Funder

Austrian Science Fund

Friedrich-Baur-Stiftung and the Fritz-Thyssen-Stiftung

NIH

Judy Seltzer Levenson Memorial Fund for CMT Research

CMT Association

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference58 articles.

1. Lower motor and primary sensory neuron diseases with peroneal muscular atrophy. I. Neurologic, genetic, and electrophysiologic findings in hereditary polyneuropathies;Dyck;Arch. Neurol.,1968