FH and hereditary leiomyomatosis and renal cell cancer: The FH-deficient fibroids included tissue from syndromic cases (truncating germline mutation [541delAG]; n = 5 from a patient with HLRCC) and non-syndromic cases (somatic missense mutation 586G > A [Ala196Thr], n = 1; somatic splice-site mutation IVS4 + 3A > G, n = 1).