RDCI, the vasoactive intestinal peptide receptor: a candidate gene for the features of Albright hereditary osteodystrophy associated with deletion of 2q37.

Albright hereditary osteodystrophy (AHO) is an autosomal dominant disorder characterised by the presence of brachymetaphalangism, short stature, obesity, and mental retardation. Variable biochemical changes many represent either pseudohypoparathyroidism (PHP) owing to resistance to parathormone (PTH...

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Bibliografiset tiedot
Päätekijät: Power, M M, James, R S, Barber, J C, Fisher, A M, Wood, P J, Leatherdale, B A, Flanagan, D E, Hatchwell, E
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 1997
Aiheet:
Research Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC1050913/
https://ncbi.nlm.nih.gov/pubmed/9138150
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