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Clinical and electrophysiological characteristics of autosomal recessive axonal Charcot-Marie-Tooth disease (ARCMT2B) that maps to chromosome 19q13.3
(Neurimuscular Disorder 14 (5) 301-306, 2004)
Cbarcot-Marie-Tooth disease (CMT) comprises a heterogeneous group of hereditary motor and sensory peripheral neuropathies. The
autosomal recessive axonal form of CMT (ARCMT2) is ram. Eight patients of a large consanguineous ...
Glaucoma in Costa RIca. Initial approaches
(2004-12-15)
El glaucoma es la segunda causa de ceguera irreversible
en el mundo. El componente genetico de algunos de
los distintos tipos ha sido demostrado: seis loci (GLC1AGLC1F)
y dos genes (TIGNMY0C y OPTN) se conocen.
hasta ...