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ABOUT JoVE

Overview Leadership Blog JoVE Help Center

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Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

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M Auranen

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Neurology|April 11, 2001

Secondary calpain3 deficiency in 2q-linked muscular dystrophy: titin is the candidate geneH Haravuori, A Vihola, V Straub, et al.

Neurology|August 28, 2002

Narrowing in on the causative defect of an intriguing X-linked myopathy with excessive autophagyB A Minassian, R Aiyar, S Alic, et al.

American Journal of Human Genetics|August 27, 1998

Genetic background of congenital chloride diarrhea in high-incidence populations: Finland, Poland, and Saudi Arabia and KuwaitP Höglund, M Auranen, J Socha, et al.

Muscle & Nerve|March 1, 2005

Enrichment of the R77C alpha-sarcoglycan gene mutation in Finnish LGMD2D patientsP Hackman, V Juvonen, J Sarparanta, et al.

Pageof 2

Search research articles

Showing results (11-20 of 14) with videos related to

Sort By:

Pageof 2

You have reached the last page of results.This site can display upto 14 results.

Neurology|April 11, 2001

Secondary calpain3 deficiency in 2q-linked muscular dystrophy: titin is the candidate geneH Haravuori, A Vihola, V Straub, et al.

Neurology|August 28, 2002

Narrowing in on the causative defect of an intriguing X-linked myopathy with excessive autophagyB A Minassian, R Aiyar, S Alic, et al.

American Journal of Human Genetics|August 27, 1998

Genetic background of congenital chloride diarrhea in high-incidence populations: Finland, Poland, and Saudi Arabia and KuwaitP Höglund, M Auranen, J Socha, et al.

Muscle & Nerve|March 1, 2005

Enrichment of the R77C alpha-sarcoglycan gene mutation in Finnish LGMD2D patientsP Hackman, V Juvonen, J Sarparanta, et al.

Pageof 2