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Neuromuscular Disorders
Volume 17, Issue 7
, Pages
547-557
, July 2007
Variable penetrance of COL6A1 null mutations: Implications for prenatal diagnosis and genetic counselling in Ullrich congenital muscular dystrophy families
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PII: S0960-8966(07)00115-0
doi: 10.1016/j.nmd.2007.03.017
© 2007 Elsevier B.V. All rights reserved.
« Previous
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Neuromuscular Disorders
Volume 17, Issue 7
, Pages
547-557
, July 2007
