A gene for autosomal recessive nemaline myopathy assigned to chromosome 2q by linkage analysis

[1]  M. Zeviani,et al.  Order of six loci at 2q24-q31 and orientation of the HOXD locus. , 1994, Genomics.

[2]  Christine E. Seidman,et al.  α-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: A disease of the sarcomere , 1994, Cell.

[3]  Cécile Fizames,et al.  The 1993–94 Généthon human genetic linkage map , 1994, Nature Genetics.

[4]  A. Beggs,et al.  Exclusion of two candidate loci for autosomal recessive nemaline myopathy. , 1994, Journal of medical genetics.

[5]  E. Haan,et al.  Assignment of a gene (NEMI) for autosomal dominant nemaline myopathy to chromosome I. , 1992, American journal of human genetics.

[6]  C. Wallgren‐Pettersson,et al.  Genetics of congenital nemaline myopathy: a study of 10 families. , 1990, Journal of medical genetics.

[7]  C. Wallgren‐Pettersson.  Congenital nemaline myopathy A clinical follow-up study of twelve patients , 1989, Journal of the Neurological Sciences.

[8]  Geraedts Jp.  Methods in molecular genetics , 1987 .

[9]  J. Ott.  Analysis of Human Genetic Linkage , 1985 .

[10]  W. Arts,et al.  Investigations on the inheritance of nemaline myopathy. , 1978, Archives of neurology.

[11]  J. Lindsey,et al.  Nemaline myopathy. A long-term clinicopathologic study of affected mother and daughter. , 1966, Brain : a journal of neurology.

[12]  A. Spiro,et al.  HEREDITARY OCCURRENCE OF NEMALINE MYOPATHY. , 1965, Archives of neurology.

[13]  W. Engel,et al.  NEMALINE MYOPATHY. A NEW CONGENITAL MYOPATHY. , 1963, Brain : a journal of neurology.

[14]  Donohue Wl,et al.  LIGHT AND ELECTRON MICROSCOPIC STUDIES OF "MYOGRANULES" IN A CHILD WITH HYPOTONIA AND MUSCLE WEAKNESS. , 1963 .

[15]  E. Haan,et al.  A mutation in the α tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathy , 1995, Nature Genetics.

[16]  N. Laing,et al.  Assignment of the human beta tropomyosin gene (TPM2) to band 9p13 by fluorescence in situ hybridisation. , 1995, Cytogenetics and cell genetics.

[17]  V. McKusick.  Mendelian Inheritance in Man: A Catalog of Human Genes and Genetic Disorders , 1997 .

[18]  S. Naylor,et al.  Report of the Fourth International Workshop on Human Chromosome 2 Mapping 1996 , 1992 .