Mudd’s disease (MAT I/III deficiency): a survey of data for MAT1A homozygotes and compound heterozygotes-Reference-Cited by-同舟云学术

Mudd’s disease (MAT I/III deficiency): a survey of data for MAT1A homozygotes and compound heterozygotes

Published:2015-08-20 Issue:1 Volume:10 Page:
ISSN:1750-1172
Container-title:Orphanet Journal of Rare Diseases
language:en
Short-container-title:Orphanet J Rare Dis

Author:

Chien Yin-Hsiu,Abdenur Jose E.,Baronio Federico,Bannick Allison Anne,Corrales Fernando,Couce Maria,Donner Markus G.,Ficicioglu Can,Freehauf Cynthia,Frithiof Deborah,Gotway Garrett,Hirabayashi Koichi,Hofstede Floris,Hoganson George,Hwu Wuh-Liang,James Philip,Kim Sook,Korman Stanley H.,Lachmann Robin,Levy Harvey,Lindner Martin,Lykopoulou Lilia,Mayatepek Ertan,Muntau Ania,Okano Yoshiyuki,Raymond Kimiyo,Rubio-Gozalbo Estela,Scholl-Bürgi Sabine,Schulze Andreas,Singh Rani,Stabler Sally,Stuy Mary,Thomas Janet,Wagner Conrad,Wilson William G.,Wortmann Saskia,Yamamoto Shigenori,Pao Maryland,Blom Henk J.

Funder

National Institute of Mental Health and by the Intramural Research Program of the NIMH

E-HOD project

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Genetics (clinical),General Medicine

Link

http://link.springer.com/content/pdf/10.1186/s13023-015-0321-y

Reference82 articles.

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