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Kallmann Syndrome Due to a Homozygous Missense c.217C>T (p.R73C) Mutation Detected in the Exon-2 of the PROK2 Gene | ESPE2016
Mehmet Nuri Ozturk; Huseyin Demirbilek; Leman Damla Kotan; Birsen Baysal; Murat Ocal; Ali Kemal Topaloglu
Published: 2016-08-19

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