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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
Kallmann Syndrome Due to a Homozygous Missense c.217C>T (p.R73C) Mutation Detected in the Exon-2 of the PROK2 Gene
2016
Mehmet Nuri Ozturk
Huseyin Demirbilek
Leman Damla Kotan
Birsen Baysal
Murat Ocal
Ali Kemal Topaloglu
Keywords:
Exon
Missense mutation
Kallmann syndrome
Genetics
Biology
Mutation
PROK2 gene
Correction
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