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489421.
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489422.
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489427.
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489428.
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Survey of somatic mutations in tuberous sclerosis complex (TSC) hamartomas suggests different genetic mechanisms for pathogenesis of TSC lesions. [electronic resource] by
- Niida, Y
- Stemmer-Rachamimov, A O
- Logrip, M
- Tapon, D
- Perez, R
- Kwiatkowski, D J
- Sims, K
- MacCollin, M
- Louis, D N
- Ramesh, V
Producer: 20010906
In:
American journal of human genetics vol. 69
Availability: No items available.
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489429.
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MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice, is mutated in autosomal dominant nonsyndromic hearing loss. [electronic resource] by
- Melchionda, S
- Ahituv, N
- Bisceglia, L
- Sobe, T
- Glaser, F
- Rabionet, R
- Arbones, M L
- Notarangelo, A
- Di Iorio, E
- Carella, M
- Zelante, L
- Estivill, X
- Avraham, K B
- Gasparini, P
Producer: 20010906
In:
American journal of human genetics vol. 69
Availability: No items available.
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