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Comment

. 2012 Jul;22(7):669-70; author reply 670-1.

doi: 10.1016/j.nmd.2012.03.007. Epub 2012 May 16.

CAV3 T78M mutation as polymorphic variant in South Italy

Patrizia Spadafora, Maria Liguori, Virginia Andreoli, Aldo Quattrone, Antonio Gambardella

PMID: 22595201
DOI: 10.1016/j.nmd.2012.03.007

Comment

CAV3 T78M mutation as polymorphic variant in South Italy

Patrizia Spadafora et al. Neuromuscul Disord. 2012 Jul.

. 2012 Jul;22(7):669-70; author reply 670-1.

doi: 10.1016/j.nmd.2012.03.007. Epub 2012 May 16.

Authors

Patrizia Spadafora, Maria Liguori, Virginia Andreoli, Aldo Quattrone, Antonio Gambardella

PMID: 22595201
DOI: 10.1016/j.nmd.2012.03.007

No abstract available

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Comment on

Rippling muscle disease and facioscapulohumeral dystrophy-like phenotype in a patient carrying a heterozygous CAV3 T78M mutation and a D4Z4 partial deletion: Further evidence for "double trouble" overlapping syndromes.
Ricci G, Scionti I, Alì G, Volpi L, Zampa V, Fanin M, Angelini C, Politano L, Tupler R, Siciliano G. Ricci G, et al. Neuromuscul Disord. 2012 Jun;22(6):534-40. doi: 10.1016/j.nmd.2011.12.001. Epub 2012 Jan 14. Neuromuscul Disord. 2012. PMID: 22245016 Free PMC article.

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