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pro vyhledávání: '"Acarsoz D"'
Autor:
Savas, S, Eraslan, S, Kantarci, S, Karaman, B, Acarsoz, D, Tukel, T, Cogulu, O, Özkınay, F, Basaran, S, Aydinli, K, Yuksel-Apak, M, Kirdar, B
WOS: 000177443300012
PubMed ID: 12210580
Childhood-onset spinal muscular atrophy (SMA) is one of the most common neurodegenerative genetic disorders. SMN1 is the SMA-determining gene deleted or mutated in the majority of SMA cases. There is
PubMed ID: 12210580
Childhood-onset spinal muscular atrophy (SMA) is one of the most common neurodegenerative genetic disorders. SMN1 is the SMA-determining gene deleted or mutated in the majority of SMA cases. There is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______9436::098afa8557fe694401a0fa66eb9f4db1
https://hdl.handle.net/11454/37290
https://hdl.handle.net/11454/37290
Autor:
Savas, S., Eraslan, S., Kantarci, S., Karaman, B., Acarsoz, D., Tükel, T., Cogulu, O., Ozkinay, F., Basaran, S., Aydınlı, K., Yuksel-Apak, M., Kirdar, B.
Publikováno v:
Prenatal Diagnosis; Aug2002, Vol. 22 Issue 8, p703-709, 7p