Hereditary Sensory Neuropathy Type I: Haplotype Analysis Shows Founders in Southern England and Europe
Author:
Publisher
Elsevier BV
Subject
Genetics(clinical),Genetics
Reference18 articles.
1. Ulcero-mutilating neuropathy in an Austrian kinship without linkage to hereditary motor and sensory neuropathy IIB and hereditary sensory neuropathy I loci;Auer-Grumbach;Neurology,2000
2. Confirmation of linkage of type 1 hereditary sensory neuropathy to human chromosome 9q22;Bejaoui;Neurology,1999
3. A YAC-based transcript map of human chromosome 9q22.1-q22.3 encompassing the loci for hereditary sensory neuropathy type I and multiple self-healing squamous epithelioma;Blair;Genomics,1998
4. Sensory radicular neuropathy associated with muscle wasting in two cases;Campbell;Brain,1964
5. Mutations in SPTLC1, encoding serine palmitoyltransferase, long chain base subunit-1, cause hereditary sensory neuropathy type I;Dawkins;Nat Genet,2001
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