Severe Dejerine‐Sottas disease with respiratory failure and dysmorphic features in association with a PMP22 point mutation and a 3q23 microdeletion
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T. Kleefstra | B. V. van Engelen | H. Houlden | B. Faas | A. Pandraud | J. Polke | M. Reilly | N. Voermans | E. Kamsteeg | M. Laurá | F. van Ruissen | A. Gabreëls-Festen