Autosomal recessive hereditary neuropathy with focally folded myelin sheaths and linked to chromosome 11q23: a distinct and homogeneous entity
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A. Brice | T. Maisonobe | D. Grid | E. Leguern | J. Urtizberea | A. Guilbot | T. Hamadouche | A. Tahan | M. Salih | M. Kabiraj | M. A. Rayess | M. Al-Turaiki | M. Akbar