The Role of a Novel TRMT1 Gene Mutation and Rare GRM1 Gene Defect in Intellectual Disability in Two Azeri Families

Behzad Davarniya; Hao Hu; Kimia Kahrizi; Luciana Musante; Zohreh Fattahi; Masoumeh Hosseini; Fariba Maqsoud; Reza Farajollahi; Thomas F. Wienker; H. Hilger Ropers; Hossein Najmabadi

doi:10.1371/journal.pone.0129631

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Open Access

Peer-reviewed

Research Article

The Role of a Novel TRMT1 Gene Mutation and Rare GRM1 Gene Defect in Intellectual Disability in Two Azeri Families

Behzad Davarniya ,

Contributed equally to this work with: Behzad Davarniya, Hao Hu

Affiliation Genetics Research Center (GRC), University of Social Welfare and Rehabilitation Sciences, Tehran, Iran
⨯
Hao Hu ,

Contributed equally to this work with: Behzad Davarniya, Hao Hu

Affiliation Department of Human Molecular Genetics, Max-Plank Institute for Molecular Genetics, Berlin, Germany
⨯
Kimia Kahrizi,

Affiliation Genetics Research Center (GRC), University of Social Welfare and Rehabilitation Sciences, Tehran, Iran
⨯
Luciana Musante,

Affiliation Department of Human Molecular Genetics, Max-Plank Institute for Molecular Genetics, Berlin, Germany
⨯
Zohreh Fattahi,

Affiliation Genetics Research Center (GRC), University of Social Welfare and Rehabilitation Sciences, Tehran, Iran
⨯
Masoumeh Hosseini,

Affiliation Genetics Research Center (GRC), University of Social Welfare and Rehabilitation Sciences, Tehran, Iran
⨯
Fariba Maqsoud,

Affiliation Welfare Organization of Ardabil Province, Ardabil, Iran
⨯
Reza Farajollahi,

Affiliation Welfare Organization of Ardabil Province, Ardabil, Iran
⨯
Thomas F. Wienker,

Affiliation Department of Human Molecular Genetics, Max-Plank Institute for Molecular Genetics, Berlin, Germany
⨯
H. Hilger Ropers,

Affiliation Department of Human Molecular Genetics, Max-Plank Institute for Molecular Genetics, Berlin, Germany
⨯
Hossein Najmabadi

* E-mail: hnajm12@yahoo.com

Affiliation Genetics Research Center (GRC), University of Social Welfare and Rehabilitation Sciences, Tehran, Iran
⨯

The Role of a Novel TRMT1 Gene Mutation and Rare GRM1 Gene Defect in Intellectual Disability in Two Azeri Families

Behzad Davarniya,
Hao Hu,
Kimia Kahrizi,
Luciana Musante,
Zohreh Fattahi,
Masoumeh Hosseini,
Fariba Maqsoud,
Reza Farajollahi,
Thomas F. Wienker,
H. Hilger Ropers

Published: August 26, 2015
https://doi.org/10.1371/journal.pone.0129631

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