Concepedia

A new phenotype of autosomal dominant nemaline myopathy

I.M.P. Gommans, Baziel G.M. van Engelen, H. J. ter Laak, Han G. Brunner, Hannie Kremer, Martin Lammens, O.J.M. Vogels

Neuromuscular Disorders · 2002 · 35 citations · 17 references

DOI

Concepts

References

17

Strategies for multilocus linkage analysis in humans.

G.M. Lathrop, J.-M. Lalouel, Cécile Julier et al. · Proceedings of the National Academy of Sciences · 1984 · 2.6K citations · Full text

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Easy calculations of lod scores and genetic risks on small computers.

G.M. Lathrop, J.-M. Lalouel · PubMed · 1984 · 1.5K citations

, , +13

Faster sequential genetic linkage computations.

Robert W. Cottingham, Ramana M. Idury, Alejandro A. Schäffer · PubMed · 1993 · 1.4K citations

, , +7

Mutations in the skeletal muscle α-actin gene in patients with actin myopathy and nemaline myopathy

Duangrurdee Wattanasirichaigoon, Hans H. Goebel, Matthew C. J. Wilce et al. · Nature Genetics · 1999 · 401 citations

, , +13

A mutation in the α tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathy

Nigel G. Laing, P. Anthony Akkari, S.M. Dorosz et al. · Nature Genetics · 1995 · 355 citations

, , +8