Variants in the PNPLA1 Gene in Families with Autosomal Recessive Congenital Ichthyosis Reveal Clinical Significance.
- DOI
- 10.1159/000516943
- Published
- 2021 Oct
- Container
- Molecular syndromology
- Publisher
- Not recorded
- Open access
- yes
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Cite this work
BibTeX
@article{allodium:10.1159/000516943,
title = {Variants in the PNPLA1 Gene in Families with Autosomal Recessive Congenital Ichthyosis Reveal Clinical Significance.},
author = {Ahmad F and Ahmed I and Alam Q and Ahmad T and Khan A and Ahmad I and Bilal M and Hayat A and Khan A and Waqas A and Rafeeq MM and Sain ZM and Umair M},
year = {2021},
journal = {Molecular syndromology},
doi = {10.1159/000516943},
url = {https://doi.org/10.1159/000516943}
}RIS
TY - JOUR TI - Variants in the PNPLA1 Gene in Families with Autosomal Recessive Congenital Ichthyosis Reveal Clinical Significance. AU - Ahmad F AU - Ahmed I AU - Alam Q AU - Ahmad T AU - Khan A AU - Ahmad I AU - Bilal M AU - Hayat A AU - Khan A AU - Waqas A AU - Rafeeq MM AU - Sain ZM AU - Umair M PY - 2021 JO - Molecular syndromology DO - 10.1159/000516943 UR - https://doi.org/10.1159/000516943 ER -
APA
F, A., I, A., Q, A., T, A., A, K., I, A., M, B., A, H., A, K., A, W., MM, R., ZM, S., & M, U. (2021). Variants in the PNPLA1 Gene in Families with Autosomal Recessive Congenital Ichthyosis Reveal Clinical Significance.. Molecular syndromology. https://doi.org/10.1159/000516943
Source records
- pubmed · retrieved 2026-09-26T04:35:48.259Z