TY  - GEN
AU  - Oliaei,Farshid
AU  - Narimani,Hossein
TI  - Bardet-Biedl 9 Syndrome, A Rare Mutation
SN  - 1735-8604
PY  - 2021///0510
KW  - Bardet-Biedl Syndrome
KW  - complications
KW  - Cilia
KW  - pathology
KW  - Cytoskeletal Proteins
KW  - genetics
KW  - Fingers
KW  - abnormalities
KW  - Genotype
KW  - Humans
KW  - Hyperparathyroidism
KW  - etiology
KW  - Hypogonadism
KW  - Iran
KW  - Kidney
KW  - Male
KW  - Middle Aged
KW  - Mutation
KW  - Polydactyly
KW  - Uremia
N1  - Publication Type: Case Reports; Journal Article
ER  -