Intronic deletions in the SLC34A3 gene: a cautionary tale for mutation analysis of hereditary hypophosphatemic rickets with hypercalciuria

Authors

Shoji Ichikawa
Shamir Tuchman, George Washington University
Leah R. Padgett
Amie K. Gray
H. Jorge Baluarte
Michael J. Econs

Document Type

Journal Article

Publication Date

2-2014

Journal

Bone

Volume

Volume 59

Inclusive Pages

53-56

Keywords

Familial Hypophosphatemic Rickets--complications; Familial Hypophosphatemic Rickets--genetics; Hypercalciuria--complications; Hypercalciuria--genetics; Introns--genetics; Sequence Deletion--genetics; Sodium-Phosphate Cotransporter Proteins, Type IIc--genetics

Comments

PMCID: PMC3903128 [Available on 2015/2/1]

APA Citation

Ichikawa, S., Tuchman, S., Padgett, R., Gray, A.K., Baluarte, H.J. et al. (2014). Intronic deletions in the SLC34A3 gene: a cautionary tale for mutation analysis of hereditary hypophosphatemic rickets with hypercalciuria. Bone, 59, 53-56.

Peer Reviewed

1