M. Folcher

Type de document

Co-auteur

C. Rivolta

L. Zografos

F. Usman

M. Ullah

A. Ullah

A. Schalenbourg

B. Royer-Bertrand

D. Rimoldi

N. Riggi

A.U. Rehman

A. Rashid

M. Quinodoz

V.G. Peter

R. Pescini-Gobert

M. Nicolas

A.-P. Moulin

S. Leyvraz

B. Khan

I. El Zaoui

K. Cisarova

M. Ansar

Date

Source

Serveur académique Lausannois (2)

Mot-clé

mutation (2) gène (2) ADN (2) Genes (2) Human beings (2) Eye (2) DNA (2) Mutation (2) puits (1) tissu (corporel) (1) spectacle (1) pipeline (1) association (1) mutant (1) paysage (1) analyse (1) famille (1) maladie (1) ligne (1) point (1) classification (1) analyse (1) cancer (1) Deletion (1) Causes (1) Cancer (1) Phenotype (1) Cyclic nucleotide phosphodiesterases (1) RNA splicing (1) Variations (1)

Documents écrit par M. Folcher (2) | parle de M. Folcher (0)

A Novel Intronic Deletion in PDE6B Causes Autosomal Recessive Retinitis Pigmentosa by Interfering with RNA Splicing.

M. Ullah et al. (2023)

Genomic and transcriptomic landscape of conjunctival melanoma.

K. Cisarova et al.