A case of Kallmann syndrome associated to a novel missense mutation of the FGFR1 gene.

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Bibliographic Details
Title: A case of Kallmann syndrome associated to a novel missense mutation of the FGFR1 gene.
Authors: Scavone M; Unit of Pediatric, University 'Magna Graecia' of Catanzaro, Catanzaro, Italy. mar.scavone@gmail.com., Chiarello P, Talarico V, Mascaro I, Caglioti C, Galati MC, Raiola G
Source: Acta bio-medica : Atenei Parmensis [Acta Biomed] 2019 Dec 23; Vol. 90 (4), pp. 577-579. Date of Electronic Publication: 2019 Dec 23.
Publication Type: Case Reports; Journal Article
Journal Info: Publisher: Mattioli 1885 Country of Publication: Italy NLM ID: 101295064 Publication Model: Electronic Cited Medium: Internet ISSN: 2531-6745 (Electronic) Linking ISSN: 03924203 NLM ISO Abbreviation: Acta Biomed Subsets: MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:2531-6745
DOI:10.23750/abm.v90i4.7170