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Hereditary motor and sensory neuropathy (HMSN) type X1 in an Argentinean family reveals independent GJB1/Cx32 mutations at the identical nucleotide position
✍ Scribed by Gerding, Wanda Maria; Koetting, Judith; Rey, Lucía Paola; Bibas Bonet, Hilda; Abdala, Mirta Esther; Mazzeo, Anna; Mostacciuolo, Maria Luisa; Arning, Larissa; Carrero-Valenzuela, Roque
- Book ID
- 123266613
- Publisher
- Elsevier Science
- Year
- 2013
- Tongue
- English
- Weight
- 463 KB
- Volume
- 27
- Category
- Article
- ISSN
- 0890-8508
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