Boucher Neuhäuser Syndrome - A rare cause of inherited hypogonadotropic hypogonadism. A case of two adult siblings with two novel mutations in PNPLA6.
| Image |  |
|---|---|
| Description | scientific article published on 16 November 2016 |
| Author/s |
author: Anja L Frederiksen Jakob H Langdahl |
| Publication date | November 16, 2016 |
| Language | |
| Country of origin | |
| Wikipedia link | |
| Copyright status | |
| Missing/wrong data? | Edit Wikidata item |