𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Linkage of autosomal dominant common variable immunodeficiency to chromosome 5p and evidence for locus heterogeneity

✍ Scribed by D. U. Braig; A. A. Schäffer; E. Glocker; U. Salzer; K. Warnatz; H. H. Peter; B. Grimbacher


Publisher
Springer
Year
2003
Tongue
English
Weight
241 KB
Volume
112
Category
Article
ISSN
0340-6717

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


No evidence for linkage of autosomal dom
✍ Katrin Kausch; Clemens R. Müller; Tiemo Grimm; Kenneth Ricker; Marcella Rietsche 📂 Article 📅 1991 🏛 Springer 🌐 English ⚖ 127 KB

Two recent articles have reported the linkage of a gene for recessive spinal muscular atrophy (SMA) on the chromosome region 5q11.2-13.3. Our data show no linkage of the dominantly inherited forms of SMA to this chromosome region.

No evidence for linkage of long QT syndr
✍ Yu-Lin Ko; Shih-Ann Chen; Tang K. Tang; Jiunn-Lee Lin; Chern-En Chiang; Jin-Jer 📂 Article 📅 1994 🏛 Springer 🌐 English ⚖ 298 KB

Recently the defective gene locus in seven Caucasian families with the Romano-Ward form of long QT syndrome (LQT) has been mapped to chromosome 1 l p. To understand the molecular basis of LQT in Chinese, a three-generation family was investigated. Fourteen family members were studied and five indivi