P.F. Chinnery

Type de document

Co-auteur

M. Yagi

S.B. Wortmann

T. Uchiumi

K. Thompson

R.W. Taylor

T.M. Strom

W. Sperl

M. Sciacco

D. Ronchi

P. Rebelo-Guiomar

H. Prokisch

G. Pierre

M. Oláhová

Y. Okazaki

A. Ohtake

K. Murayama

V.K. Mootha

M. Moggio

M. Minczuk

T. Meitinger

J.A. Mayr

E. Mastantuono

R.N. Lightowlers

L.S. Kremer

R. Kopajtich

M. Kohda

J. Koch

Y. Kishita

D. Kang

A.A. Jourdain

C. Garone

R.G. Feichtinger

S. DiMauro

D'Souza, A.R.

G.P. Comi

Z.M. Chrzanowska-Lightowlers

S.E. Calvo

C.L. Alston

Date

Source

Serveur académique Lausannois (1)

Mot-clé

nourisson (1) protéine (1) mutation (1) infection (1) importation (1) maladie humaine (1) enzyme (1) embryon (1) ADN (1) âge (1) enfant (1) adulte (1) règlement (1) index (1) jeune (1) Defects (1) Complement (1) Showing (1) Forms (1) Cases (1) Phenotype (1) Mitochondrial DNA (1) Apoptosis (1) Proteins--Conformation (1) Transcription (1) Scarcity (1) Phosphorylation (1) Muscles--Diseases (1) Mitochondria (1) Mice (1)

Documents écrit par P.F. Chinnery (1) | parle de P.F. Chinnery (0)

Biallelic C1QBP Mutations Cause Severe Neonatal-, Childhood-, or Later-Onset Cardiomyopathy Associated with Combined Respiratory-Chain Deficiencies.

R.G. Feichtinger et al. (5 oct. 2017)