A distinct congenital motor and sensory neuropathy (neuronal type) with dysmorphic features in a father and two sons. A variant of Charcot-Marie-Tooth disease
Ruiz, C, Rivas, F, Ramírez-Casillas, G, Vázquez-Santana, R, Mendoza-Chalita, B, Feria-Velasco, A, Tapia-Arizmendi, G, Cantú, J M
Published in Clinical genetics (01.02.1987)
Published in Clinical genetics (01.02.1987)
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Journal Article
A novel Leu171Pro mutation in presenilin-1 gene in a Mexican family with early onset Alzheimer disease
Ramirez-Dueñas, M G, Rogaeva, E A, Leal, C A, Lin, C, Ramirez-Casillas, G A, Hernandez-Romo, J A, St George-Hyslop, P H, Cantu, J M
Published in Annales de génétique (1998)
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Published in Annales de génétique (1998)
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