De Sandre-Giovannoli, A., Chaouch, M., Kozlov, S., Vallat, J., Tazir, M., Kassouri, N., . . . Lévy, N. (2002). 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 Society of Human Genetics.
Citação norma ChicagoDe Sandre-Giovannoli, Annachiara, et al. 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 Society of Human Genetics, 2002.
Citação norma MLADe Sandre-Giovannoli, Annachiara, et al. 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 Society of Human Genetics, 2002.