Genetic mapping of the mouse neuromuscular mutation kyphoscoliosis
Author:
Publisher
Elsevier BV
Subject
Genetics
Reference24 articles.
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1. Genotypic and phenotypic spectrum of Myofibrillar Myopathy 7 as a result of Kyphoscoliosis Peptidase deficiency: The first description of a missense mutation in KY and literature review;European Journal of Medical Genetics;2022-08
2. A new early-onset neuromuscular disorder associated with kyphoscoliosis peptidase (KY) deficiency;European Journal of Human Genetics;2016-08-03
3. Identification of a Z-band associated protein complex involving KY, FLNC and IGFN1;Experimental Cell Research;2010-07
4. Linkage analysis of genetic loci for kyphoscoliosis on chromosomes 5p13, 13q13.3, and 13q32;American Journal of Medical Genetics Part A;2006
5. Mice with a Targeted Deletion of the Tetranectin Gene Exhibit a Spinal Deformity;Molecular and Cellular Biology;2001-11-15
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