A novel CISD2 mutation associated with a classical Wolfram syndrome phenotype alters Ca2+ homeostasis and ER-mitochondria interactions.
Hum Mol Genet
; 26(9): 1599-1611, 2017 05 01.
Article
in En
| MEDLINE
| ID: mdl-28335035
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Optic Atrophy
/
Aging, Premature
/
Mitochondrial Diseases
/
Hearing Loss, Sensorineural
/
Membrane Proteins
Type of study:
Risk_factors_studies
Limits:
Humans
/
Male
/
Middle aged
Language:
En
Journal:
Hum Mol Genet
Journal subject:
BIOLOGIA MOLECULAR
/
GENETICA MEDICA
Year:
2017
Document type:
Article
Affiliation country:
Francia
Country of publication:
Reino Unido