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Mosaicism for GJB1 mutation causes milder Charcot-Marie-Tooth X1 phenotype in a heterozygous man than in a manifesting heterozygous woman.
- Published in:
- Neurogenetics, 2013, v. 14, n. 3/4, p. 189, doi. 10.1007/s10048-013-0368-7
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- Publication type:
- Article
Bronchoskopická volumredukce v kontextu fyzioterapeutických možností.
- Published in:
- Rehabilitation & Physical Medicine / Rehabilitace a Fyzikální Lékařství, 2017, v. 24, n. 4, p. 202
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- Publication type:
- Article
Paroxysmal hemipareses in childhood.
- Published in:
- 1979
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- Publication type:
- journal article