Prenatal diagnosis in laminin α2 chain (merosin)-deficient congenital muscular dystrophy: A collective experience of five international centers
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F. Muntoni | M. Zatz | N. Romero | H. Topaloglu | T. Voit | C. Sewry | S. Abbs | P. Guicheney | M. Vainzof | M. Brockington | F. Tomé | P. Richard | C. Ledeuil | B. Talim | C. Jiménez-Mallebrera | R. Herrmann | R. Mein | L. Yamamoto | H. Topaloğlu