Literature DB >> 21083612

The first report of homozygous May-Hegglin anomaly E1841K mutation.

Behzad Poopak1, Hamid Rezvani, Analisa Difeo, John A Martignetti, Gelareh Khosravipour, Abolfazl Yousefian, Kobra Farahani, Fariba Haghnejad Doshanlo, Najmaldin Saki.   

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Year:  2011        PMID： 21083612     DOI： 10.1111/j.1600-0609.2010.01553.x

Source DB:  PubMed          Journal:  Eur J Haematol        ISSN： 0902-4441            Impact factor:   2.997


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  2 in total

1.  Macrothrombocytopenia With Döhle Body-Like Granulocyte Inclusions: A Case Report of May-Hegglin Anomaly in a 33-Year-Old White Woman With an Update on the Molecular Findings of MYH9-Related Disease.

Authors:  Steven M Ruhoy; Amanda Yates
Journal:  Lab Med       Date:  2016-06-28

2.  Mouse models of MYH9-related disease: mutations in nonmuscle myosin II-A.

Authors:  Yingfan Zhang; Mary Anne Conti; Daniela Malide; Fan Dong; Aibing Wang; Yelena A Shmist; Chengyu Liu; Patricia Zerfas; Mathew P Daniels; Chi-Chao Chan; Elliot Kozin; Bechara Kachar; Michael J Kelley; Jeffrey B Kopp; Robert S Adelstein
Journal:  Blood       Date:  2011-09-08       Impact factor: 22.113
  2 in total

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