NMPhenogen: a comprehensive database for genotype-phenotype correlation in neuromuscular genetic disorders.

Manjunath U, R V, Kulkarni SS, Reddy HN, Anil A, Mishra RK, Iyer GR

DOI: 10.3389/fnins.2025.1696899
Published: 2025
Container: Frontiers in neuroscience
Publisher: Not recorded
Open access: yes

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Cite this work

BibTeX

@article{allodium:10.3389/fnins.2025.1696899,
  title = {NMPhenogen: a comprehensive database for genotype-phenotype correlation in neuromuscular genetic disorders.},
  author = {Manjunath U and R V and Kulkarni SS and Reddy HN and Anil A and Mishra RK and Iyer GR},
  year = {2025},
  journal = {Frontiers in neuroscience},
  doi = {10.3389/fnins.2025.1696899},
  url = {https://doi.org/10.3389/fnins.2025.1696899}
}

RIS

TY  - JOUR
TI  - NMPhenogen: a comprehensive database for genotype-phenotype correlation in neuromuscular genetic disorders.
AU  - Manjunath U
AU  - R V
AU  - Kulkarni SS
AU  - Reddy HN
AU  - Anil A
AU  - Mishra RK
AU  - Iyer GR
PY  - 2025
JO  - Frontiers in neuroscience
DO  - 10.3389/fnins.2025.1696899
UR  - https://doi.org/10.3389/fnins.2025.1696899
ER  -

APA

U, M., V, R., SS, K., HN, R., A, A., RK, M., & GR, I. (2025). NMPhenogen: a comprehensive database for genotype-phenotype correlation in neuromuscular genetic disorders.. Frontiers in neuroscience. https://doi.org/10.3389/fnins.2025.1696899

Source records

pubmed · retrieved 2026-09-27T08:41:34.864Z