Associated Papers
Identification and Functional Characterization of a Novel Variant in the SEMA3A Gene in a Chinese Family with Kallmann Syndrome.
Shu M et al.
International Journal of Endocrinology, 2022
SEMA3A and IGSF10 Are Novel Contributors to Combined Pituitary Hormone Deficiency (CPHD).
Budny B et al.
Frontiers in Endocrinology, 2020
Human Semaphorin 3 Variants Link Melanocortin Circuit Development and Energy Balance.
van der Klaauw AA et al.
Cell, 2019
30661757 (PubMed )
Supplement: mmc1.xlsx › Sheet1
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