These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
3. The genomic structure of the human skeletal muscle sodium channel gene. McClatchey AI; Lin CS; Wang J; Hoffman EP; Rojas C; Gusella JF Hum Mol Genet; 1992 Oct; 1(7):521-7. PubMed ID: 1339144 [TBL] [Abstract][Full Text] [Related]
4. Physical linkage of the human growth hormone gene cluster and the skeletal muscle sodium channel alpha-subunit gene (SCN4A) on chromosome 17. Bennani-Baiti IM; Jones BK; Liebhaber SA; Cooke NE Genomics; 1995 Oct; 29(3):647-52. PubMed ID: 8575757 [TBL] [Abstract][Full Text] [Related]
5. Linkage of Agt and Actsk-1 to distal mouse chromosome 8 loci: a new conserved linkage. Abonia JP; Abel KJ; Eddy RL; Elliott RW; Chapman VM; Shows TB; Gross KW Mamm Genome; 1993; 4(1):25-32. PubMed ID: 8093670 [TBL] [Abstract][Full Text] [Related]
6. Dinucleotide repeat polymorphisms at the SCN4A locus suggest allelic heterogeneity of hyperkalemic periodic paralysis and paramyotonia congenita. McClatchey AI; Trofatter J; McKenna-Yasek D; Raskind W; Bird T; Pericak-Vance M; Gilchrist J; Arahata K; Radosavljevic D; Worthen HG Am J Hum Genet; 1992 May; 50(5):896-901. PubMed ID: 1315122 [TBL] [Abstract][Full Text] [Related]
7. Three brain sodium channel alpha-subunit genes are clustered on the proximal segment of mouse chromosome 2. Malo D; Schurr E; Dorfman J; Canfield V; Levenson R; Gros P Genomics; 1991 Jul; 10(3):666-72. PubMed ID: 1679748 [TBL] [Abstract][Full Text] [Related]
8. Linkage data suggesting allelic heterogeneity for paramyotonia congenita and hyperkalemic periodic paralysis on chromosome 17. Koch MC; Ricker K; Otto M; Grimm T; Bender K; Zoll B; Harper PS; Lehmann-Horn F; RĂ¼del R; Hoffman EP Hum Genet; 1991 Nov; 88(1):71-4. PubMed ID: 1660029 [TBL] [Abstract][Full Text] [Related]
9. Paramyotonia congenita and hyperkalemic periodic paralysis are linked to the adult muscle sodium channel gene. Ebers GC; George AL; Barchi RL; Ting-Passador SS; Kallen RG; Lathrop GM; Beckmann JS; Hahn AF; Brown WF; Campbell RD Ann Neurol; 1991 Dec; 30(6):810-6. PubMed ID: 1686388 [TBL] [Abstract][Full Text] [Related]
10. A new sodium channel alpha-subunit gene (Scn9a) from Schwann cells maps to the Scn1a, Scn2a, Scn3a cluster of mouse chromosome 2. Beckers MC; Ernst E; Belcher S; Howe J; Levenson R; Gros P Genomics; 1996 Aug; 36(1):202-5. PubMed ID: 8812438 [TBL] [Abstract][Full Text] [Related]
11. A multipoint genetic linkage map of mouse chromosome 18. Johnson KR; Davisson MT Genomics; 1992 Aug; 13(4):1143-9. PubMed ID: 1354640 [TBL] [Abstract][Full Text] [Related]
12. Linkage of malignant hyperthermia and hyperkalemic periodic paralysis to the adult skeletal muscle sodium channel (SCN4A) gene in a large pedigree. Moslehi R; Langlois S; Yam I; Friedman JM Am J Med Genet; 1998 Feb; 76(1):21-7. PubMed ID: 9508059 [TBL] [Abstract][Full Text] [Related]
13. Linkage of acid alpha-glucosidase (Gaa) and thymidine kinase (Tk-1) to esterase-3 (Es-3) on mouse chromosome 11. Martiniuk F; Hirschhorn R; D'Eustachio P Mamm Genome; 1991; 1(4):267-9. PubMed ID: 1794057 [TBL] [Abstract][Full Text] [Related]
14. A novel mutation in the gene for the adult skeletal muscle sodium channel alpha-subunit (SCN4A) that causes paramyotonia congenita of von Eulenburg. Sasaki R; Takano H; Kamakura K; Kaida K; Hirata A; Saito M; Tanaka H; Kuzuhara S; Tsuji S Arch Neurol; 1999 Jun; 56(6):692-6. PubMed ID: 10369308 [TBL] [Abstract][Full Text] [Related]
15. A linkage map of mouse chromosome 19: definition of comparative mapping relationships with human chromosomes 10 and 11 including the MEN1 locus. Rochelle JM; Watson ML; Oakey RJ; Seldin MF Genomics; 1992 Sep; 14(1):26-31. PubMed ID: 1358795 [TBL] [Abstract][Full Text] [Related]
16. Mutations in the muscle sodium channel gene (SCN4A) in 13 French families with hyperkalemic periodic paralysis and paramyotonia congenita: phenotype to genotype correlations and demonstration of the predominance of two mutations. Plassart E; Reboul J; Rime CS; Recan D; Millasseau P; Eymard B; Pelletier J; Thomas C; Chapon F; Desnuelle C Eur J Hum Genet; 1994; 2(2):110-24. PubMed ID: 8044656 [TBL] [Abstract][Full Text] [Related]
17. Murine tyrosine hydroxylase maps to the distal end of chromosome 7 within a region conserved in mouse and man. Brilliant MH; Niemann MM; Eicher EM J Neurogenet; 1987 Aug; 4(5):259-66. PubMed ID: 2889817 [TBL] [Abstract][Full Text] [Related]
18. DNA variants with telomere probe enable genetic mapping of ends of mouse chromosomes. Elliott RW; Yen CH Mamm Genome; 1991; 1(2):118-22. PubMed ID: 1686839 [TBL] [Abstract][Full Text] [Related]
19. Exclusion of malignant hyperthermia susceptibility (MHS) from a putative MHS2 locus on chromosome 17q and of the alpha 1, beta 1, and gamma subunits of the dihydropyridine receptor calcium channel as candidates for the molecular defect. Sudbrak R; Golla A; Hogan K; Powers P; Gregg R; Du Chesne I; Lehmann-Horn F; Deufel T Hum Mol Genet; 1993 Jul; 2(7):857-62. PubMed ID: 8395939 [TBL] [Abstract][Full Text] [Related]