Homozygous Defects in LMNA, Encoding Lamin A/C Nuclear-Envelope Proteins, Cause Autosomal Recessive Axonal Neuropathy in Human (Charcot-Marie-Tooth Disorder Type 2) and Mouse
The American Journal of Human Genetics2002Vol. 70(3), pp. 726–736
Citations Over TimeTop 1% of 2002 papers
Annachiara De Sandre‐Giovannoli, Malika Chaouch, Serguei Kozlov, Jean-Michel Vallat, Mériem Tazir, Nadia Kassouri, Pierre Szepetowski, T. Hammadouche, Antoon Vandenberghe, Colin L. Stewart, Djamel Grid, Nicolas Lévy
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