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Unusual type of benign x-linked muscular dystrophy.
PMID: 5969090 [PubMed - indexed for MEDLINE]
PMCID: PMC1064196
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Cited by 20 PubMed Central articles
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MAN1 and emerin have overlapping function(s) essential for chromosome segregation and cell division in Caenorhabditis elegans.
Liu J, Lee KK, Segura-Totten M, Neufeld E, Wilson KL, Gruenbaum Y.
Proc Natl Acad Sci U S A. 2003 Apr 15; 100(8):4598-603. Epub 2003 Apr 8.
[Proc Natl Acad Sci U S A. 2003]
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Different mutations in the LMNA gene cause autosomal dominant and autosomal recessive Emery-Dreifuss muscular dystrophy.
Raffaele Di Barletta M, Ricci E, Galluzzi G, Tonali P, Mora M, Morandi L, Romorini A, Voit T, Orstavik KH, Merlini L, et al.
Am J Hum Genet. 2000 Apr; 66(4):1407-12. Epub 2000 Mar 16.
[Am J Hum Genet. 2000]
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Identification of a new locus for a peculiar form of congenital muscular dystrophy with early rigidity of the spine, on chromosome 1p35-36.
Moghadaszadeh B, Desguerre I, Topaloglu H, Muntoni F, Pavek S, Sewry C, Mayer M, Fardeau M, Tomé FM, Guicheney P.
Am J Hum Genet. 1998 Jun; 62(6):1439-45.
[Am J Hum Genet. 1998]
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