J. Leal Loureiro

Type de document

Co-auteur

J. Zenker

P Zavadakova

J. Weis

G. Venturini

M. Vaz Pato

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

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 J. Leal Loureiro (1) | parle de J. Leal Loureiro (0)

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

H. Azzedine et al. (2013)