Mutations in OCRL1 gene in Indian children with Lowe syndrome.

Sethi SK, Bagga A, Gulati A, Hari P, Gupta N, Lunardi J

Open source

DOI
10.1007/s10157-008-0059-0
Published
2008 Oct
Container
Clinical and experimental nephrology
Publisher
Not recorded
Open access
no

Credibility signals

limited evidence Score 43/100 under policy 1.0.0. This is a metadata assessment, not a judgment of the paper's conclusions.

Show all credibility signals

Cite this work

BibTeX

@article{allodium:10.1007/s10157-008-0059-0,
  title = {Mutations in OCRL1 gene in Indian children with Lowe syndrome.},
  author = {Sethi SK and Bagga A and Gulati A and Hari P and Gupta N and Lunardi J},
  year = {2008},
  journal = {Clinical and experimental nephrology},
  doi = {10.1007/s10157-008-0059-0},
  url = {https://doi.org/10.1007/s10157-008-0059-0}
}

RIS

TY  - JOUR
TI  - Mutations in OCRL1 gene in Indian children with Lowe syndrome.
AU  - Sethi SK
AU  - Bagga A
AU  - Gulati A
AU  - Hari P
AU  - Gupta N
AU  - Lunardi J
PY  - 2008
JO  - Clinical and experimental nephrology
DO  - 10.1007/s10157-008-0059-0
UR  - https://doi.org/10.1007/s10157-008-0059-0
ER  - 

APA

SK, S., A, B., A, G., P, H., N, G., & J, L. (2008). Mutations in OCRL1 gene in Indian children with Lowe syndrome.. Clinical and experimental nephrology. https://doi.org/10.1007/s10157-008-0059-0

Source records