| 1 | CCT5, ELP1, HSAN1, HSAN2A, HSAN3, HSAN4, HSAN5, NGF, NTRK1, SNSP, SPTLC1, WNK1
|
| Genes for hereditary sensory and autonomic neuropathies: a genotype-phenotype correlation.
|
| Rotthier A, Baets J, De Vriendt E, Jacobs A, Auer-Grumbach M, Lévy N, Bonello-Palot N, Kilic SS, Weis J, Nascimento A, Swinkels M, Kruyt MC, Jordanova A, De Jonghe P, Timmerman V.
|
| Brain 132(Pt 10):2699-711. Epub 2009 Aug 3.PMID: 19651702 2009
|
| 2 | HSAN2A, WNK1
|
| Mutations in the nervous system--specific HSN2 exon of WNK1 cause hereditary sensory neuropathy type II.
|
| Shekarabi M, Girard N, Rivière JB, Dion P, Houle M, Toulouse A, Lafrenière RG, Vercauteren F, Hince P, Laganiere J, Rochefort D, Faivre L, Samuels M, Rouleau GA.
|
| J Clin Invest 118(7):2496-505.PMID: 18521183 2008
|
| 3 | HSAN2A, WNK1
|
| Novel mutations in the HSN2 gene causing hereditary sensory and autonomic neuropathy type II.
|
| Coen K, Pareyson D, Auer-Grumbach M, Buyse G, Goemans N, Claeys KG, Verpoorten N, Laurˆ M, Scaioli V, Salmhofer W, Pieber TR, Nelis E, De Jonghe P, Timmerman V.
|
| Neurology 66(5):748-51. 2006
|
| 4 | HSAN2A, WNK1
|
| Two mutations in the HSN2 gene explain the high prevalence of HSAN2 in French Canadians.
|
| Roddier K, Thomas T, Marleau G, Gagnon AM, Dicaire MJ, St-Denis A, Gosselin I, Sarrazin AM, Larbrisseau A, Lambert M, Vanasse M, Gaudet D, Rouleau GA, Brais B.
|
| Neurology 64(10):1762-7. 2005
|
| 5 | HSAN2A, WNK1
|
| Identification of a Novel Gene (HSN2) Causing Hereditary Sensory and Autonomic Neuropathy Type II through the Study of Canadian Genetic Isolates.
|
| Lafreniere RG, MacDonald ML, Dube MP, MacFarlane J, O'Driscoll M, Brais B, Meilleur S, Brinkman RR, Dadivas O, Pape T, Platon C, Radomski C, Risler J, Thompson J, Guerra-Escobio AM, Davar G, Breakefield XO, Pimstone SN, Green R, Pryse-Phillips W, Goldberg YP, Younghusband HB, Hayden MR, Sherrington R, Rouleau GA, Samuels ME.
|
| Am J Hum Genet 74(5):1064-73. Epub 2004 Apr 01. 2004
|
| 6 | HSAN2A, WNK1
|
| A mutation in the HSN2 gene causes sensory neuropathy type II in a Lebanese family.
|
| Riviere JB, Verlaan DJ, Shekarabi M, Lafreniere RG, Benard M, Der Kaloustian VM, Shbaklo Z, Rouleau GA.
|
| Ann Neurol 56(4):572-5. 2004
|
| 7 | HSAN2A
|
| Persistent skin ulcers, mutilations, and acro-osteolysis in hereditary sensory and autonomic neuropathy with phospholipid excretion. Report of a family.
|
| Bockers M, Benes P, Bork K.
|
| J Am Acad Dermatol 21(4 Pt 1):736-9. 1989
|
| 8 | HSAN2A
|
| Hereditary sensory neuropathy, type II. Clinical, electrophysiologic, histologic, and biochemical studies of a Quebec kinship.
|
| Ota M, Ellefson RD, Lambert EH, Dyck PJ.
|
| Arch Neurol 29(1):23-37. No abstract available. 1973
|