Spondyloepimetaphyseal dysplasia, Missouri variant, is located on chromosome 11q22.3 and is caused by a mutation of matrix metalloproteinase 13 (MMP13).
Main Authors: | Kennedy, A, Christi, P, Harding, B, Pannett, A, Dearlove, A, Whyte, M, Thakker, R |
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פורמט: | Conference item |
יצא לאור: |
2002
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פריטים דומים
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MMP13 mutation causes spondyloepimetaphyseal dysplasia, Missouri type (SEMD(MO).
מאת: Kennedy, A, et al.
יצא לאור: (2005) -
Linkage studies of a Missouri kindred with autosomal dominant spondyloepimetaphyseal dysplasia (SEMD) indicate genetic heterogeneity.
מאת: Gertner, J, et al.
יצא לאור: (1997) -
Novel RPL13 variants and evidence for incomplete penetrance in a human ribosomopathy with spondyloepimetaphyseal dysplasia
מאת: Alice Costantini, et al.
יצא לאור: (2020-10-01) -
LINKAGE STUDIES IN A KINDRED WITH AUTOSOMAL-DOMINANT SPONDYLOEPIMETAPHYSEAL DYSPLASIA (SEMD) INDICATE GENETIC-HETEROGENEITY
מאת: Gertner, J, et al.
יצא לאור: (1995) -
Clinical, genetic and structural delineation of RPL13-related spondyloepimetaphyseal dysplasia suggest extra-ribosomal functions of eL13
מאת: Prince Jacob, et al.
יצא לאור: (2023-11-01)