M. Vaz Pato

Type de document

Co-auteur

J. Zenker

P Zavadakova

J. Weis

G. Venturini

A. Title

G. Stevanin

C. Stendel

J. Senderek

L. Schöls

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 M. Vaz Pato (1) | parle de M. Vaz Pato (0)

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

H. Azzedine et al. (2013)