Linkage of X-linked Myopathy with Excessive Autophagy (XMEA) to Xq28
Overview
Authors
Affiliations
X-linked myopathy with excessive autophagy (XMEA, MIM 310440) is a rare inherited mild myopathy. We have used 32 polymorphic markers spanning the entire X chromosome to exclude most of the chromosome except the Xq28 region in a large XMEA family. Using three additional families for linkage analysis, we have obtained a significant two-point lod score with marker DXS1183 (Z = 2.69 at theta = 0). Multipoint linkage analysis confirmed the assignment of the disease locus with a maximal lod score of 2.74 obtained at recombination fraction zero. Linkage of XMEA to the Xq28 region is thus firmly established. In addition, we have ruled out the Emery-Dreifuss muscular dystrophy to be allelic with XMEA by direct sequencing of the emerin gene in three of our families.
Altered muscle differentiation in X-linked myopathy with excessive autophagy.
Fernandes S, Almeida C, Souza L, Lazar M, Onofre-Oliveira P, Yamamoto G Dis Model Mech. 2019; 13(2).
PMID: 31826868 PMC: 6994946. DOI: 10.1242/dmm.041244.
Late adult-onset of X-linked myopathy with excessive autophagy.
Crockett C, Ruggieri A, Gujrati M, Zallek C, Ramachandran N, Minassian B Muscle Nerve. 2014; 50(1):138-44.
PMID: 24488655 PMC: 4589296. DOI: 10.1002/mus.24197.
The systematic functional characterisation of Xq28 genes prioritises candidate disease genes.
Kolb-Kokocinski A, Mehrle A, Bechtel S, Simpson J, Kioschis P, Wiemann S BMC Genomics. 2006; 7:29.
PMID: 16503986 PMC: 1431524. DOI: 10.1186/1471-2164-7-29.
Bornemann A, Goebel H Brain Pathol. 2001; 11(2):206-17.
PMID: 11303796 PMC: 8098536. DOI: 10.1111/j.1750-3639.2001.tb00393.x.