A case of Kallmann syndrome carrying a missense mutation in alternatively spliced exon 8A encoding the immunoglobulin-like domain IIIb of fibroblast growth factor receptor 1
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| Description | scientific article |
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author: Stephanie B Seminara Koh-ichiro Yoshiura Kiyonori Miura Hideaki Masuzaki Norio Niikawa |
| Publication date | February 6, 2010 |
| Language | English |
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| Missing/wrong data? | Edit Wikidata item |