作者
Jennifer J Johnston, Richard I Kelley, Thomas O Crawford, D Holmes Morton, Richa Agarwala, Thorsten Koch, Alejandro A Schäffer, Clair A Francomano, Leslie G Biesecker
发表日期
2000/10/1
期刊
The American Journal of Human Genetics
卷号
67
期号
4
页码范围
814-821
出版商
Elsevier
简介
The nemaline myopathies are characterized by weakness and eosinophilic, rodlike (nemaline) inclusions in muscle fibers. Amish nemaline myopathy is a form of nemaline myopathy common among the Old Order Amish. In the first months of life, affected infants have tremors with hypotonia and mild contractures of the shoulders and hips. Progressive worsening of the proximal contractures, weakness, and a pectus carinatum deformity develop before the children die of respiratory insufficiency, usually in the second year. The disorder has an incidence of ∼1 in 500 among the Amish, and it is inherited in an autosomal recessive pattern. Using a genealogy database, automated pedigree software, and linkage analysis of DNA samples from four sibships, we identified an ∼2-cM interval on chromosome 19q13.4 that was homozygous in all affected individuals. The gene for the sarcomeric thin-filament protein, slow …
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JJ Johnston, RI Kelley, TO Crawford, DH Morton… - The American Journal of Human Genetics, 2000