Rare Diseases
Records 1 - 2 (of 2 Records) |
Query Trace: Charcot-marie-tooth Disease Type 1[original query]>>Original Studies[Product Type] |
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Expanding the spectrum of KIF5A mutations-case report of a large kindred with familial ALS and overlapping syndrome. Dulski JarosLaw et al. Amyotrophic lateral sclerosis & frontotemporal degeneration 2023 1-4 |
Genetic testing practices for Charcot-Marie-Tooth type 1A disease. |