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C M Castelein Selected Research

Cochleosaccular degeneration of the inner ear and progressive cataracts

11/2000Human nonsyndromic hereditary deafness DFNA17 is due to a mutation in nonmuscle myosin MYH9.

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C M Castelein Research Topics

Disease

1MYH9-Related Disorders
11/2000
1Cochleosaccular degeneration of the inner ear and progressive cataracts
11/2000
1Deafness (Deaf Mutism)
11/2000
1Hearing Loss (Hearing Impairment)
11/2000

Drug/Important Bio-Agent (IBA)

1A 17 (A-17)IBA
11/2000
1Adenosine Triphosphatases (ATPase)IBA
11/2000
1Amino AcidsFDA Link
11/2000
1Myosins (Myosin)IBA
11/2000
1NucleotidesIBA
11/2000
1Myosin Heavy Chains (Myosin Heavy Chain)IBA
11/2000
1Myosin Type IIIBA
11/2000