K.H. Sonoda

Discipline

Psychologie (1)

Type de document

Co-auteur

Y. Wada

C. Rivolta

K.M. Nishiguchi

K. Nikopoulos

T. Nakazawa

Y. Ikeda

N.L. Wesseling

S.K. Verbakel

RAC van Huet

S. Ueno

H. Terasaki

C. Terao

A.U. Rehman

M. Quinodoz

A. Prunotto

A.S. Plomp

A. Murakami

N. Miyake

F. Miya

N. Matsumoto

Z. Kutalik

M. Kubo

H. Koskiniemi-Kuendig

B.J. Klevering

CCW Klaver

M.I. Khan

E. Kersten

Y. Kamatani

T. Ishibashi

C.B. Hoyng

M.J. Geerlings

N. Fuse

P. Farinelli

A.I. den Hollander

FPM Cremers

K. Cisarova

CJF Boon

AAB Bergen

M. Akiyama

Date

Source

Serveur académique Lausannois (2)

Mot-clé

gène (2) maladie (2) Retinal (Visual pigment) (2) Patients (2) Patients (2) maladie (2) puits (1) thérapie (1) acte législatif (1) spectacle (1) association (1) mutation (1) modèle (1) champ (1) enrichissement (1) âge (1) Treatment (1) Case (1) Diseases (1) Phenotype (1) Visual acuity (1) Therapeutics (1) Social groups (1) Series (1) Retinitis pigmentosa (1) Population (1) Nonsense mutation (1) Medical records (1) Japanese (1) Heterozygosity (1)

Documents écrit par K.H. Sonoda (2) | parle de K.H. Sonoda (0)

A frequent variant in the Japanese population determines quasi-Mendelian inheritance of rare retinal ciliopathy.

K. Nikopoulos et al. (28 juin 2019)

Macular Dystrophy and Cone-Rod Dystrophy Caused by Mutations in the RP1 Gene: Extending the RP1 Disease Spectrum.

S.K. Verbakel et al. (2019)