Simard L R, Vanasse M, Rochette C, Morgan K, Lemieux B, Melançon S B, Labuda D
Génétique Médicale, Centre de Recherche, Hôpital Sainte-Justine, Université de Montréal, Québec, Canada.
Genomics. 1992 Sep;14(1):188-90. doi: 10.1016/s0888-7543(05)80305-2.
Chronic childhood-onset spinal muscular atrophy (SMA) is, after Duchenne muscular dystrophy, the most common neuromuscular disorder in childhood. Recent linkage analyses have mapped this disease to 5q12-5q14. We show that chronic SMA (Types II and III) is tightly linked to the marker locus D5S39 (Zmax = 5.47 at theta = 0.02) in eight French Canadian families. In contrast to previously published results, we do not observe close linkage between chronic SMA and D5S6 (Zmax = 0.34 at theta = 0.18) or D5S78 (Zmax = 0.25 at theta = 0.21). Last, we present a family that appears to be discordant for this localization but may represent the first example of an incompletely penetrant individual.