skip to main content
Lingue:
Filtrati per: Lista di tutte le versioni rimuovi
Result Number Material Type Add to My Shelf Action Record Details and Options
1
Material Type:
Articolo
Aggiungi allo Scaffale Elettronico

Absence of an orphan mitochondrial protein, C19orf12, causes a distinct clinical subtype of neurodegenration with brain iron accumulation.(Report)

Hartig, Monika B. ; Jurkiewicz, Elzbieta ; Dusi, Sabrina ; Winkelmann, Juliane ; Mueller - Felber, Wolfgang ; Kretzschmar, Hans ; Iuso, Arcangela ; Heim, Katharina ; Krajewska - Walasek, Malgorzata ; Elstner, Matthias ; Gasser, Thomas ; Schmitz, Gerd ; Haack, Tobias ; Roeber, Sigrun ; Jozwiak, Sergiusz ; Oexle, Konrad ; Trenkwalder, Claudia ; Strom, Tim M. ; Kmiec, Tomasz ; Tarabin, Victoria ; Hempel, Maja ; Klopstock, Thomas ; Tiranti, Valeria ; Meitinger, Thomas ; Prokisch, Holger

American Journal of Human Genetics, Oct 7, 2011, Vol.89(4), p.543(8) [Rivista Peer Reviewed]

Cengage Learning, Inc.

Accesso online

2
Material Type:
Articolo
Aggiungi allo Scaffale Elettronico

Absence of an orphan mitochondrial protein, C19orf12, causes a distinct clinical subtype of neurodegenration with brain iron accumulation.(Report)

Hartig, Monika B. ; Jurkiewicz, Elzbieta ; Dusi, Sabrina ; Winkelmann, Juliane ; Mueller - Felber, Wolfgang ; Kretzschmar, Hans ; Iuso, Arcangela ; Heim, Katharina ; Krajewska - Walasek, Malgorzata ; Elstner, Matthias ; Gasser, Thomas ; Schmitz, Gerd ; Haack, Tobias ; Roeber, Sigrun ; Jozwiak, Sergiusz ; Oexle, Konrad ; Trenkwalder, Claudia ; Strom, Tim M. ; Kmiec, Tomasz ; Tarabin, Victoria ; Hempel, Maja ; Klopstock, Thomas ; Tiranti, Valeria ; Meitinger, Thomas ; Prokisch, Holger

American Journal of Human Genetics, Oct 7, 2011, Vol.89(4), p.543(8) [Rivista Peer Reviewed]

Cengage Learning, Inc.

Accesso online

3
Material Type:
Articolo
Aggiungi allo Scaffale Elettronico

Absence of an Orphan Mitochondrial Protein, C19orf12, Causes a Distinct Clinical Subtype of Neurodegeneration with Brain Iron Accumulation

Hartig, Monika b ; Iuso, Arcangela ; Haack, Tobias ; Kmiec, Tomasz ; Jurkiewicz, Elzbieta ; Heim, Katharina ; Roeber, Sigrun ; Tarabin, Victoria ; Dusi, Sabrina ; Krajewska-Walasek, Malgorzata ; Jozwiak, Sergiusz ; Hempel, Maja ; Winkelmann, Juliane ; Elstner, Matthias ; Oexle, Konrad ; Klopstock, Thomas ; Mueller-Felber, Wolfgang ; Gasser, Thomas ; Trenkwalder, Claudia

The American Journal of Human Genetics, 2011, Vol.89(4), pp.543-550 [Rivista Peer Reviewed]

ScienceDirect Journals (Elsevier)

Accesso online

4
Absence of an Orphan Mitochondrial Protein, C19orf12, Causes a Distinct Clinical Subtype of Neurodegeneration with Brain Iron Accumulation
Material Type:
Articolo
Aggiungi allo Scaffale Elettronico

Absence of an Orphan Mitochondrial Protein, C19orf12, Causes a Distinct Clinical Subtype of Neurodegeneration with Brain Iron Accumulation

Hartig, Monika b. ; Iuso, Arcangela ; Haack, Tobias ; Kmiec, Tomasz ; Jurkiewicz, Elzbieta ; Heim, Katharina ; Roeber, Sigrun ; Tarabin, Victoria ; Dusi, Sabrina ; Krajewska-Walasek, Malgorzata ; Jozwiak, Sergiusz ; Hempel, Maja ; Winkelmann, Juliane ; Elstner, Matthias ; Oexle, Konrad ; Klopstock, Thomas ; Mueller-Felber, Wolfgang ; Gasser, Thomas ; Trenkwalder, Claudia ; Tiranti, Valeria ; Kretzschmar, Hans ; Schmitz, Gerd ; Strom, Tim m. ; Meitinger, Thomas ; Prokisch, Holger

The American Journal of Human Genetics, 10/2011, Vol.89(4), pp.543-550 [Rivista Peer Reviewed]

Elsevier (via CrossRef)

Accesso online

5
Material Type:
Articolo
Aggiungi allo Scaffale Elettronico

Absence of an orphan mitochondrial protein, c19orf12, causes a distinct clinical subtype of neurodegeneration with brain iron accumulation

Hartig, Monika B ; Iuso, Arcangela ; Haack, Tobias ; Kmiec, Tomasz ; Jurkiewicz, Elzbieta ; Heim, Katharina ; Roeber, Sigrun ; Tarabin, Victoria ; Dusi, Sabrina ; Krajewska-Walasek, Malgorzata ; Jozwiak, Sergiusz ; Hempel, Maja ; Winkelmann, Juliane ; Elstner, Matthias ; Oexle, Konrad ; Klopstock, Thomas ; Mueller-Felber, Wolfgang ; Gasser, Thomas ; Trenkwalder, Claudia ; Tiranti

American journal of human genetics, 07 October 2011, Vol.89(4), pp.543-50 [Rivista Peer Reviewed]

MEDLINE/PubMed (U.S. National Library of Medicine)

Accesso online

Personalizza i tuoi risultati

  1. Edita

Refine Search Results

Espandi i miei risultati

  1.   

Ricerca in corso nelle risorse remote ...