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

✍ Scribed by Annachiara De Sandre-Giovannoli; Malika Chaouch; Serguei Kozlov; Jean-Michel Vallat; Meriem Tazir; Nadia Kassouri; Pierre Szepetowski; Tarik Hammadouche; Antoon Vandenberghe; Colin L. Stewart; Djamel Grid; Nicolas Lévy

• Book ID: 117853841
• Publisher: American Society of Human Genetics
• Year: 2002
• Tongue: English
• Weight: 980 KB
• Volume: 70
• Category: Article
• ISSN: 0002-9297
• DOI: 10.1086/339274