Unique three-site compound heterozygous mutation in the WFS1 gene in Wolfram syndrome.

Ren Z, Yi J, Zhong M, Wang Y, Liu Q, Wang X, Liu D, Ren W

DOI: 10.1186/s12902-021-00823-5
Published: 2021 Aug 17
Container: BMC endocrine disorders
Publisher: Not recorded
Open access: yes

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Cite this work

BibTeX

@article{allodium:10.1186/s12902-021-00823-5,
  title = {Unique three-site compound heterozygous mutation in the WFS1 gene in Wolfram syndrome.},
  author = {Ren Z and Yi J and Zhong M and Wang Y and Liu Q and Wang X and Liu D and Ren W},
  year = {2021},
  journal = {BMC endocrine disorders},
  doi = {10.1186/s12902-021-00823-5},
  url = {https://doi.org/10.1186/s12902-021-00823-5}
}

RIS

TY  - JOUR
TI  - Unique three-site compound heterozygous mutation in the WFS1 gene in Wolfram syndrome.
AU  - Ren Z
AU  - Yi J
AU  - Zhong M
AU  - Wang Y
AU  - Liu Q
AU  - Wang X
AU  - Liu D
AU  - Ren W
PY  - 2021
JO  - BMC endocrine disorders
DO  - 10.1186/s12902-021-00823-5
UR  - https://doi.org/10.1186/s12902-021-00823-5
ER  -

APA

Z, R., J, Y., M, Z., Y, W., Q, L., X, W., D, L., & W, R. (2021). Unique three-site compound heterozygous mutation in the WFS1 gene in Wolfram syndrome.. BMC endocrine disorders. https://doi.org/10.1186/s12902-021-00823-5

Source records

pubmed · retrieved 2026-09-27T07:31:44.081Z