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Fh-Souassi: a founder frameshift mutation in exon 10 of the LDL-receptor gene, associated with a mild phenotype in Tunisian families

✍ Scribed by M.N. Slimane; S. Lestavel; X.-M. Sun; F. Maatouk; A.K. Soutar; M.H. Ben Farhat; V. Clavey; P. Benlian; M. Hammami

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

A point mutation in the low density lipo

✍ X.-M. Sun; D.D. Patel; S. McCarthy; B.L. Knight; A.K. Soutar 📂 Article 📅 1994 🏛 Elsevier Science 🌐 English ⚖ 145 KB

Premature termination mutations in exon

✍ Sossi, Vittorio; Giuli, Anna; Vitali, Tiziana; Tiziano, Francesco; Mirabella, Ma 📂 Article 📅 2001 🏛 Nature Publishing Group 🌐 English ⚖ 228 KB

Association of an Exon 3 Mutation (Trp66

✍ Emile Levy; Anne Minnich; Suzanne Lussier Cacan; Louise Thibault; Louise-Marie G 📂 Article 📅 1997 🏛 Elsevier Science 🌐 English ⚖ 152 KB

Mutation screening of the LDLR gene and

✍ Henrik Nissen; Sophie Lestavel; Torben Stiig Hansen; Gérald Luc; Eric Bruckert; 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 371 KB

A novel mutation in Exon 4 of the low de

✍ Barbara A. Morash; Meng-Hee Tan; Bassam A. Nassar; Catherine K.L. Too; Duane L. 📂 Article 📅 1998 🏛 Elsevier Science 🌐 English ⚖ 209 KB