A Presumed Synonymous Mutation of PKD2 Caused Autosomal Dominant Polycystic Kidney Disease in a Chinese Family.
Curr Med Sci
; 41(5): 1029-1036, 2021 Oct.
Article
in En
| MEDLINE
| ID: mdl-34542828
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Polycystic Kidney, Autosomal Dominant
/
TRPP Cation Channels
/
Silent Mutation
/
Solitary Kidney
/
Exome Sequencing
Type of study:
Prognostic_studies
Limits:
Adult
/
Child
/
Female
/
Humans
/
Male
/
Middle aged
Country/Region as subject:
Asia
Language:
En
Journal:
Curr Med Sci
Year:
2021
Document type:
Article
Affiliation country: