Varaico: Literature-Extracted Genetic Variants

Gene:FGF17
Variant:p.R96Q
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FGF17

NM_003867.4:p.R96Q

Associated Papers

Genetic spectrum of Kallmann syndrome: Single-center experience and systematic review.

Patil VA et al.

Clinical Endocrinology, 2022

36138264 (PubMed )
Supplement: supplement_1.xlsx › Sheet1

Congenital hypogonadotropic hypogonadism and constitutional delay of growth and puberty have distinct genetic architectures.

Cassatella D et al.

European Journal of Endocrinology, 2018

29419413 (PubMed )
Supplement: eje-178-377-t002.pdf
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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."