Novel mutation in OCRL leading to a severe form of Lowe syndrome.

Zhou FQ, Wang QW, Liu ZZ, Zhang XL, Wang DN, Dongye MM, Lin HT, Chen WR

DOI: 10.18240/ijo.2019.07.01
Published: 2019
Container: International journal of ophthalmology
Publisher: Not recorded
Open access: yes

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Cite this work

BibTeX

@article{allodium:10.18240/ijo.2019.07.01,
  title = {Novel mutation in OCRL leading to a severe form of Lowe syndrome.},
  author = {Zhou FQ and Wang QW and Liu ZZ and Zhang XL and Wang DN and Dongye MM and Lin HT and Chen WR},
  year = {2019},
  journal = {International journal of ophthalmology},
  doi = {10.18240/ijo.2019.07.01},
  url = {https://doi.org/10.18240/ijo.2019.07.01}
}

RIS

TY  - JOUR
TI  - Novel mutation in OCRL leading to a severe form of Lowe syndrome.
AU  - Zhou FQ
AU  - Wang QW
AU  - Liu ZZ
AU  - Zhang XL
AU  - Wang DN
AU  - Dongye MM
AU  - Lin HT
AU  - Chen WR
PY  - 2019
JO  - International journal of ophthalmology
DO  - 10.18240/ijo.2019.07.01
UR  - https://doi.org/10.18240/ijo.2019.07.01
ER  -

APA

FQ, Z., QW, W., ZZ, L., XL, Z., DN, W., MM, D., HT, L., & WR, C. (2019). Novel mutation in OCRL leading to a severe form of Lowe syndrome.. International journal of ophthalmology. https://doi.org/10.18240/ijo.2019.07.01

Source records

pubmed · retrieved 2026-09-26T06:47:56.303Z