Old Web
English
Sign In
Acemap
>
Paper
>
CC2D2A mutations lead to variable phenotypes in a family with retinal dystrophy
CC2D2A mutations lead to variable phenotypes in a family with retinal dystrophy
2017
Cécile Méjécase
Saddek Mohand-Said
Camille Andrieux
Aurélie Hummel
Said El Shamieh
Aline Antonio
Fiona Boyard
Christel Condroyer
Christelle Michiels
Steven B. Blanchard
Mélanie Letexier
Jean-Paul Saraiva
José-Alain Sahel
Christina Zeitz
Isabelle Audo
Keywords:
Phenotype
retinal dystrophy
Diabetes mellitus
CC2D2A
Genetics
Biology
Anatomy
Correction
Source
Cite
Save
Machine Reading By IdeaReader
0
References
2
Citations
NaN
KQI
[]