| S. Farinon < S. Fauré < S. Fauset | Facettes : |
List of bibliographic references
Number of relevant bibliographic references: 1.| Ident. | Authors (with country if any) | Title |
|---|---|---|
| 003A11 (1995) | C. Wallgren-Pettersson [Finlande] ; K. Avela [Finlande] ; S. Marchand [France] ; J. Kolehmainen [Finlande] ; E. Tahvanainen [Finlande] ; F. Juul Hansen [Danemark] ; F. Muntoni [Royaume-Uni] ; V. Dubowitz [Royaume-Uni] ; M. De Visser [Pays-Bas] ; I. M. Van Langen [Pays-Bas] ; Nigel G. Laing [Finlande] ; S. Fauré [Australie] ; A. De La Chapelle [Finlande] | A gene for autosomal recessive nemaline myopathy assigned to chromosome 2q by linkage analysis |
List of associated KwdEn.i
| Nombre de documents | Descripteur |
|---|---|
| 1 | Autosomal |
| 1 | Autosomal recessive nemaline myopathy |
| 1 | Chromosome |
| 1 | Congenital |
| 1 | Congenital nemaline myopathy |
| 1 | Gene tpm3 |
| 1 | Genet |
| 1 | Genetics |
| 1 | Helsinki |
| 1 | Laing |
| 1 | Linkage |
| 1 | Linkage analysis |
| 1 | Medical genetics |
| 1 | Muscle fibres |
| 1 | Muscle weakness |
| 1 | Mutation |
| 1 | Myopathy |
| 1 | Nem2 |
| 1 | Nem2 gene |
| 1 | Nemaline |
| 1 | Nemaline bodies |
| 1 | Nemaline myopathy |
| 1 | Recessive |
| 1 | Tpm3 |
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EXPLOR_STEP=$WICRI_ROOT/Wicri/Asie/explor/AustralieFrV1/Data/UK/Analysis
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HfdIndexSelect -h $EXPLOR_AREA/Data/UK/Analysis/Author.i \
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