Novel compound heterozygous mutations in ENPP1 cause hypophosphataemic rickets with anterior spinal ligament ossification.
主要な著者: | Mehta, P, Mitchell, A, Tysoe, C, Caswell, R, Owens, M, Vincent, T |
---|---|
フォーマット: | Journal article |
言語: | English |
出版事項: |
2012
|
類似資料
-
Windswept lower limb deformities in patients with hypophosphataemic rickets
著者:: Ali Al Kaissi, 等
出版事項: (2013-12-01) -
Seven novel mutations in the PEX gene indicate molecular heterogeneity for X-linked hypophosphataemic rickets.
著者:: Dixon, P, 等
出版事項: (1996) -
Mapping of human X-linked hypophosphataemic rickets by multilocus linkage analysis.
著者:: Read, A, 等
出版事項: (1986) -
X-linked hypophosphataemic rickets due to pseudo-exons of the PHEX gene.
著者:: Christie, P, 等
出版事項: (2000) -
Bridging markers defining the map position of X linked hypophosphataemic rickets.
著者:: Thakker, R, 等
出版事項: (1987)