Boucher Neuhäuser Syndrome - A rare cause of inherited hypogonadotropic hypogonadism: A case of two adult siblings with two novel mutations in PNPLA6

Jakob Høgild Langdahl, Anja Lisbeth Frederiksen, Nina N. T. T. Nguyen, Klaus Brusgaard, Claus Bogh Juhl

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Medicin og biovidenskab