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Article

X-linked hypophosphatemia. A phenotype in search of a cause.

The International journal of biochemistry - 1 May 1992

Tenenhouse H S, Scriver C R

Abstract excerpt

XLH is an important disease, it is the subject of several classic articles in the medical sciences (Scriver et al., 1991), and it has been an important stimulus to study renal hypophosphatemias and how they are involved in rickets and osteomalacia (Scriver, 1974; Scriver and Tenenhouse, 1991). Renal transport is the major determinant of phosphate homeostasis in mammals and it is unlikely that this important...

Topics

Animals
Genetic Linkage
Humans
Hypophosphatemia, Familial
Kidney
Mutation
Phenotype
X Chromosome

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 1592145
DOI: 10.1016/0020-711x(92)90001-h

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 29 Aug 2026. Prepared record publication-1592145-2026-08-29.1. Manifest publication-graph-cohort-2026-08-29.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 29 Aug 2026.

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