Comment on "Congenital Hypogonadotropic Hypogonadism with Anosmia and Gorlin Features Caused by a PTCH1 Mutation Reveals a New Candidate Gene for Kallmann Syndrome" (Barraud et al., Neuroendocrinology, 2021;111:99-114).
- DOI
- 10.1159/nen/advag003
- Published
- 2026 Sep 9
- Container
- Neuroendocrinology
- Publisher
- Not recorded
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1159/nen/advag003,
title = {Comment on "Congenital Hypogonadotropic Hypogonadism with Anosmia and Gorlin Features Caused by a PTCH1 Mutation Reveals a New Candidate Gene for Kallmann Syndrome" (Barraud et al., Neuroendocrinology, 2021;111:99-114).},
author = {Hercent A and Tchernitchko D},
year = {2026},
journal = {Neuroendocrinology},
doi = {10.1159/nen/advag003},
url = {https://doi.org/10.1159/nen/advag003}
}RIS
TY - JOUR TI - Comment on "Congenital Hypogonadotropic Hypogonadism with Anosmia and Gorlin Features Caused by a PTCH1 Mutation Reveals a New Candidate Gene for Kallmann Syndrome" (Barraud et al., Neuroendocrinology, 2021;111:99-114). AU - Hercent A AU - Tchernitchko D PY - 2026 JO - Neuroendocrinology DO - 10.1159/nen/advag003 UR - https://doi.org/10.1159/nen/advag003 ER -
APA
A, H., & D, T. (2026). Comment on "Congenital Hypogonadotropic Hypogonadism with Anosmia and Gorlin Features Caused by a PTCH1 Mutation Reveals a New Candidate Gene for Kallmann Syndrome" (Barraud et al., Neuroendocrinology, 2021;111:99-114).. Neuroendocrinology. https://doi.org/10.1159/nen/advag003
Source records
- pubmed · retrieved 2026-09-26T04:24:17.029Z