Identification of the gene whose mutation leads to hypocoptyl tropism inArabidopsis thaliana
β Scribed by O. A. Ogarkova; A. A. Tomilov; N. B. Tomilova; V. A. Tarasov
- Publisher
- SP MAIK Nauka/Interperiodica
- Year
- 2005
- Tongue
- English
- Weight
- 58 KB
- Volume
- 41
- Category
- Article
- ISSN
- 1022-7954
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
Mutations in the gene encoding fibrillin-1 (FBN1) cause Marfan syndrome (MFS) and other related connective tissue disorders. In this study we performed SSCP to analyze all 65 exons of the FBN1 gene in 76 patients presenting with classical MFS or related phenotypes. We report 7 missense mutations, 3
Communicated by
A heterozygous deletion of exon 9 in the COL1A2 -mRNA of a patient with symptoms of both the Ehlers -Danlos -Syndrome and the Osteogenesis Imperfecta is described. In the genomic DNA of the patient, exon 9 is homozygously present. We identified a novel heterozygous point mutation in the splice donor