S. Micheal

Type de document

Co-auteur

M. Ueffing

M.K. Tsilimbaris

C. Tsika

R. Roepman

C. Rivolta

S. Plainis

K. Nikopoulos

A.P. Moulin

A. Messina

M.K. Mbefo

U. Kjellström

M.I. Khan

B. Giangreco

P. Farinelli

I. El Zaoui

S.A. Di Gioia

S. Decembrini

F.P. Cremers

K. Cisarova

K. Boldt

S.V. Blazaki

N. Bedoni

S. Balzano

Y. Arsenijevic

S. Andréasson

Date

Source

Serveur académique Lausannois (1)

Mot-clé

peau (1) protéine (1) mutation (1) morphologie (1) île (1) analyse (1) gène (1) maladie (1) sujet (1) taux (1) Morphology (1) Defects (1) Control (1) Vision (1) Usher's syndrome (1) Skin (1) Scarcity (1) RNA (1) Retinitis pigmentosa (1) Retinal degeneration (1) Retinal (Visual pigment) (1) Protein binding (1) Photoreceptors (1) Nature (1) Morphology (1) Mice (1) Human beings (1) Hearing (1) Fibroblasts (1) Families (1)

Documents écrit par S. Micheal (1) | parle de S. Micheal (0)

Mutations in CEP78 Cause Cone-Rod Dystrophy and Hearing Loss Associated with Primary-Cilia Defects.

K. Nikopoulos et al. (1 sept. 2016)