L. Schöls

Type de document

Co-auteur

J. Zenker

P Zavadakova

J. Weis

G. Venturini

M. Vaz Pato

A. Title

G. Stevanin

C. Stendel

J. Senderek

G. Said

A. Roos

C. Rivolta

O. Poirot

V. Planté-Bordeneuve

N. Pinto

J.J. Médard

E. Makowski

E. Leguern

J. Leal Loureiro

O. Dubourg

K.G. Claeys

R. Chrast

R. Cartoni

N. Bernard-Marissal

L. Bartesaghi

J. Baraban

H. Azzedine

E. Arnaud Gouttenoire

A. Amato

Date

Source

Serveur académique Lausannois (1)

Mot-clé

région (1) besoin (1) mutation (1) perte (1) plomb (1) analyse (1) gène (1) maladie (1) Observations (1) Observations (1) Identification (1) Abnormalities (1) Genes (1) Scarcity (1) Neurons (1) Neuroglia (1) Neural conduction (1) Nerves, Peripheral--Diseases (1) Nerves, Peripheral (1) Muscles (1) Mice (1) Lead (1) Identification (1) Foot (1) Farm produce (1) Families (1) Children (1) Charcot-Marie-Tooth disease (1) Abnormalities, Human (1) Ability (1)

Documents écrit par L. Schöls (1) | parle de L. Schöls (0)

PLEKHG5 deficiency leads to an intermediate form of autosomal-recessive Charcot-Marie-Tooth disease.

H. Azzedine et al. (2013)