E. Banin

Type de document

Co-auteur

D. Sharon

C. Rivolta

T. Ben-Yosef

E. Zampaglione

A.R. Webster

N.E. Wagner

A.B. Sousa

R. Sangermano

F.P. Ruberto

B. Rosin

M. Quinodoz

E.M. Place

E. A. Pierce

V.G. Peter

R. Pescini-Gobert

A. Obolensky

M Neves

P. Namburi

M. Michaelides

A. Larson

A. Kimchi

R.M. Huckfeldt

A.B. Fulton

V. Dunet

I. Deitch

L. Coutinho Santos

K.M. Bujakowska

S. Balzano

R. Ba-Abbad

G. Arno

A. AlTalbishi

Date

Source

Serveur académique Lausannois (2)

Mot-clé

gène (2) Reporting (2) Patients (2) Families (2) Evidence (2) Patients (2) région (1) protéine (1) association (1) carte (1) plomb (1) histoire (1) analyse (1) ADN (1) maladie (1) investigation (1) Decay (1) Defects (1) History (1) Parts (1) Parts (1) Identification (1) Description and travel (1) Cases (1) Social groups (1) Retinitis pigmentosa (1) Retinal (Visual pigment) (1) Perimetry (1) Modeling (1) Messenger RNA (1)

Documents écrit par E. Banin (2) | parle de E. Banin (0)

Broadening INPP5E phenotypic spectrum: detection of rare variants in syndromic and non-syndromic IRD.

R. Sangermano et al. (29 juin 2021)

Heterozygous deletions of noncoding parts of the PRPF31 gene cause retinitis pigmentosa via reduced gene expression.

F.P. Ruberto et al. (2021)