A nonsense mutation ofPEPD in four Amish children with prolidase deficiency-Reference-Cited by-同舟云学术

A nonsense mutation ofPEPD in four Amish children with prolidase deficiency

Published:2006 Issue:6 Volume:140A Page:580-585
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Wang Heng,Kurien Biji T.,Lundgren David,Patel Nisha C.,Kaufman K. M.,Miller David L.,Porter Andrew C.,D'Souza Anil,Nye Leah,Tumbush John,Hupertz Vera,Kerr Douglas S.,Kurono S.,Matsumoto H.,Scofield R. Hal

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference34 articles.

1. Blood transfusions in the therapy of a case of prolidase deficiency

2. Prolidase deficiency: A multisystemic hereditary disorder

3. Prolidase deficiency: case reports of two Argentinian brothers

4. Mild, late-onset prolidase deficiency: another Italian case

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