Associated Papers
Functional characterization of all missense variants in LEPR, PCSK1, and POMC genes arising from single-nucleotide variants.
Shah BP et al.
Expert Review of Endocrinology & Metabolism, 2023
36864747 (PubMed )
Supplement: supplement_1.zip › supple_PPL › PPL_Variant_Supp3-POMC-OR.xlsx › Sheet1
Clinical and mutation analysis of four Chinese families with von Hippel-Lindau disease.
Chen J et al.
Clinical & Translational Oncology : Official Publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico, 2013
[Family survey and clinical analysis of von Hippel-Lindau syndrome].
Chen JM et al.
Zhonghua Wai Ke Za Zhi [chinese Journal of Surgery], 2012
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