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Related Articles by Review for PMID: 19308961
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A broad spectrum of developmental delay in a large cohort of prolidase deficiency patients demonstrates marked interfamilial and intrafamilial phenotypic variability.
Am J Med Genet B Neuropsychiatr Genet. 2010 Jan 5;153B(1):46-56. doi: 10.1002/ajmg.b.30945.
Am J Med Genet B Neuropsychiatr Genet. 2010.
PMID: 19308961
Molecular basis of prolidase (peptidase D) deficiency.
Endo F, Matsuda I.
Endo F, et al.
Mol Biol Med. 1991 Feb;8(1):117-27.
Mol Biol Med. 1991.
PMID: 1943683
Review.
Item in Clipboard
Human prolidase and prolidase deficiency: an overview on the characterization of the enzyme involved in proline recycling and on the effects of its mutations.
Lupi A, Tenni R, Rossi A, Cetta G, Forlino A.
Lupi A, et al.
Amino Acids. 2008 Nov;35(4):739-52. doi: 10.1007/s00726-008-0055-4. Epub 2008 Mar 14.
Amino Acids. 2008.
PMID: 18340504
Review.
Item in Clipboard
Biotechnological applications of recombinant microbial prolidases.
Theriot CM, Tove SR, Grunden AM.
Theriot CM, et al.
Adv Appl Microbiol. 2009;68:99-132. doi: 10.1016/S0065-2164(09)01203-9.
Adv Appl Microbiol. 2009.
PMID: 19426854
Review.
Item in Clipboard
A novel WDR62 missense mutation in microcephaly with abnormal cortical architecture and review of the literature.
Zombor M, Kalmár T, Nagy N, Berényi M, Telcs B, Maróti Z, Brandau O, Sztriha L.
Zombor M, et al.
J Appl Genet. 2019 May;60(2):151-162. doi: 10.1007/s13353-019-00486-y. Epub 2019 Feb 1.
J Appl Genet. 2019.
PMID: 30706430
Review.
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