Type II hyperprolinaemia in a pedigree of Irish travellers (nomads).

Author:

Flynn M P,Martin M C,Moore P T,Stafford J A,Fleming G A,Phang J M

Publisher

BMJ

Subject

Pediatrics, Perinatology, and Child Health

Reference25 articles.

1. Disorders of proline and hydroxyproline metabolism;Scriver, C.R.; Smith, R.J.; Phang, J.M.,1983

2. Renal tubular transport of proline, hydroxyproline and glycine in health and in familial hyperprolinemia;Scriver, C.R.; Efron, M.L.; Schafer, I.A.;J Clin Invest,1964

3. Maternal hyperprolinaemia;Whelan, D.T.; Connor, W.T.;Lancet,1980

4. Metabolism of prolines and the hydroxyprolines;Adams, E.; Frank, A.;Annu Rev Biochem,1980

5. Familial hyperprolinemia, cerebral dysfunction and renal anomalies occurring in a family with hereditary nephropathy and deafness;Schafer, I.A.; Scriver, C.R.; Efron, M.L.;N Engl J Med,1962

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