X-linked vacuolar myopathies: Two separate loci and refined genetic mapping

Annals of Neurology

Volumn 47, Issue 5, 2000, Pages 666-669

  Auranen, Mari ^a   Villanova, Marcello ^b   Muntoni, Francesco ^c   Fardeau, Michel ^d   Scherer, Stephen W ^f   Kalino, Hannu ^g   Minassian, Berge A ^e,f  

^a NATIONAL PUBLIC HEALTH INSTITUTE   (Finland)

^b Lab di Patologia Neuromuscolare   (Italy)

^c HAMMERSMITH HOSPITAL   (United Kingdom)

^d PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

^e UNIVERSITY OF TORONTO   (Canada)

^f HOSPITAL FOR SICK CHILDREN   (Canada)

^g TURKU UNIVERSITY HOSPITAL   (Finland)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOPHAGY; CARDIOMYOPATHY; CHROMOSOME MARKER; GENE LOCUS; GENE MAPPING; GENETIC LINKAGE; HUMAN; MALE; MENTAL DEFICIENCY; MYOPATHY; PRIORITY JOURNAL; X CHROMOSOME LINKED DISORDER;

ADOLESCENT; ADULT; CHROMOSOME MAPPING; FEMALE; HAPLOTYPES; HUMANS; LINKAGE (GENETICS); MALE; MICROSATELLITE REPEATS; MYOPATHIES, STRUCTURAL, CONGENITAL; PEDIGREE; VACUOLES; X CHROMOSOME;

EID: 0034098689     PISSN: 03645134     EISSN: None     Source Type: Journal    
DOI: 10.1002/1531-8249(200005)47:5<666::AID-ANA19>3.0.CO;2-N     Document Type: Article

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