anchor instance (Q102982)

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    p.R85C variant has been described in a heterozygous state in patients with idiopathic hypogonadotropic
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    , Kallmann syndrome, healthy first-degree relatives of Kallmann probands, and rare healthy controls.
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    1,060
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    14
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    24,508
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    17 April 2019
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    Digenic Inheritance of PROKR2 and WDR11 Mutations in Pituitary Stalk Interruption Syndrome. (5505202)
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