A broad spectrum of developmental delay in a large cohort of prolidase deficiency patients demonstrates marked interfamilial and intrafamilial phenotypic variability-Reference-Cited by-同舟云学术

A broad spectrum of developmental delay in a large cohort of prolidase deficiency patients demonstrates marked interfamilial and intrafamilial phenotypic variability

Published:2009 Issue: Volume:9999B Page:n/a-n/a
ISSN:1552-4841
Container-title:American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Falik-Zaccai Tzipora C.,Khayat Morad,Luder Anthony,Frenkel Pnina,Magen Daniella,Brik Riva,Gershoni-Baruch Ruth,Mandel Hanna

Publisher

Wiley

Subject

Cellular and Molecular Neuroscience,Psychiatry and Mental health,Genetics (clinical)

Reference30 articles.

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5. Systemic lupus erythematosus-like disease in a 6-year-old boy with prolidase deficiency;Di Rocco;J Inherit Metab Dis,2007

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