Seri, M <br/><br/>
Mutations in MYH9 result in the May-Hegglin anomaly, and Fechtner and Sebastian syndromes. The May-Heggllin/Fechtner Syndrome Consortium.  [electronic resource] 

 -  Nature genetics  Sep 2000 
 - 103-5 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>1061-4036 
<br/><br/><label>Standard No.: </label>10.1038/79063  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Alleles<br/>Amino Acid Sequence<br/>Animals<br/>Blood Platelet Disorders--genetics<br/>Cataract--genetics<br/>Chickens<br/>Chromosomes, Human, Pair 22<br/>Crystallography, X-Ray<br/>Cytoplasm--metabolism<br/>Genotype<br/>Hearing Loss, Sensorineural--genetics<br/>Humans<br/>Leukocytes--pathology<br/>Models, Molecular<br/>Molecular Motor Proteins<br/>Molecular Sequence Data<br/>Muscle, Smooth--metabolism<br/>Mutation<br/>Mutation, Missense<br/>Myosin Heavy Chains--chemistry<br/>Myosins--chemistry<br/>Nephritis--genetics<br/>Neutrophils--pathology<br/>Phenotype<br/>Protein Conformation<br/>Protein Structure, Tertiary<br/>Sequence Homology, Amino Acid<br/>Syndrome<br/>Thrombocytopenia--genetics