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 (Q24632769)
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Current Data About 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
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(P1932) Annachiara De Sandre-Giovannoli
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(P1476) "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" (language: en)

(P2093) Malika Chaouch
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Serguei Kozlov
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Jean-Michel Vallat
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Meriem Tazir
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Nadia Kassouri
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Tarik Hammadouche
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Antoon Vandenberghe
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Colin L Stewart
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Djamel Grid
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Nicolas Lévy
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(P356) 10.1086/339274
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