Lataa...
Congenital myotonic dystrophy in Britain. II. Genetic basis.
Genetic analysis of 54 sibships containing 70 patients with congenital myotonic dystrophy has shown paternal transmission in only one case, the disorder being maternally transmitted in 51 sibships. No instance of new mutation was found. At least half the sibs were unaffected; 9 sibs were affected wi...
Tallennettuna:
| Päätekijä: | |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
1975
|
| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1544592/ https://ncbi.nlm.nih.gov/pubmed/1167063 |
| Tagit: |
Lisää tagi
Ei tageja, Lisää ensimmäinen tagi!
|