MYH9 gene mutations associated with bleeding

Research output: Contribution to journalArticle

7 Citations (Scopus)
Original languageEnglish
Pages (from-to)312-315
Number of pages4
JournalPlatelets
Volume28
Issue number3
DOIs
Publication statusPublished - May 2017

Keywords

  • Asymptomatic Diseases
  • Blood Platelets/metabolism
  • Cell Size
  • Chromosomes, Human, Pair 22/chemistry
  • Exons
  • Gene Expression
  • Genetic Association Studies
  • Genotype
  • Hearing Loss, Sensorineural/genetics
  • Hemorrhage/genetics
  • Humans
  • Molecular Motor Proteins/genetics
  • Mutation
  • Myosin Heavy Chains/genetics
  • Phenotype
  • Platelet Count
  • Protein Domains
  • Severity of Illness Index
  • Thrombocytopenia/congenital

Cite this

MYH9 gene mutations associated with bleeding. / Savoia, Anna; De Rocco, Daniela; Pecci, Alessandro.

In: Platelets, Vol. 28, No. 3, 05.2017, p. 312-315.

Research output: Contribution to journalArticle

@article{ae8d8c5beb9e452b866ed4c5abd38706,
title = "MYH9 gene mutations associated with bleeding",
keywords = "Asymptomatic Diseases, Blood Platelets/metabolism, Cell Size, Chromosomes, Human, Pair 22/chemistry, Exons, Gene Expression, Genetic Association Studies, Genotype, Hearing Loss, Sensorineural/genetics, Hemorrhage/genetics, Humans, Molecular Motor Proteins/genetics, Mutation, Myosin Heavy Chains/genetics, Phenotype, Platelet Count, Protein Domains, Severity of Illness Index, Thrombocytopenia/congenital",
author = "Anna Savoia and {De Rocco}, Daniela and Alessandro Pecci",
year = "2017",
month = "5",
doi = "10.1080/09537104.2017.1294250",
language = "English",
volume = "28",
pages = "312--315",
journal = "Platelets",
issn = "0953-7104",
publisher = "Taylor & Francis",
number = "3",

}

TY - JOUR

T1 - MYH9 gene mutations associated with bleeding

AU - Savoia, Anna

AU - De Rocco, Daniela

AU - Pecci, Alessandro

PY - 2017/5

Y1 - 2017/5

KW - Asymptomatic Diseases

KW - Blood Platelets/metabolism

KW - Cell Size

KW - Chromosomes, Human, Pair 22/chemistry

KW - Exons

KW - Gene Expression

KW - Genetic Association Studies

KW - Genotype

KW - Hearing Loss, Sensorineural/genetics

KW - Hemorrhage/genetics

KW - Humans

KW - Molecular Motor Proteins/genetics

KW - Mutation

KW - Myosin Heavy Chains/genetics

KW - Phenotype

KW - Platelet Count

KW - Protein Domains

KW - Severity of Illness Index

KW - Thrombocytopenia/congenital

U2 - 10.1080/09537104.2017.1294250

DO - 10.1080/09537104.2017.1294250

M3 - Article

VL - 28

SP - 312

EP - 315

JO - Platelets

JF - Platelets

SN - 0953-7104

IS - 3

ER -