References for disease Familial restrictive cardiomyopathy 2

All publications related to disease Familial restrictive cardiomyopathy 2. To link directly to a specific first author surname click on the required letter below.

DP

D

Dunand M, Lobrinus JA, Jeannet PY, Behin A, Claeys KG, Selcen D, Kuntzer T
Confirmation that abnormal desmin accumulation and migration are due to a desmin gene mutation in a familial cardiomyopathy and distal myopathy.
Neuromuscul Disord 2009 () - PubMed: 19716701

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P

Pruszczyk P, Kostera-Pruszczyk A, Shatunov A, Goudeau B, Dramiñska A, Takeda K, Sambuughin N, Vicart P, Strelkov SV, Goldfarb LG, Kamiñska A
Restrictive cardiomyopathy with atrioventricular conduction block resulting from a desmin mutation.
Int J Cardiol 2007 117(2) 244-253 PubMed: 16890305

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This page was last modified: April 17 2009 14:28:35.