Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Raluca Anca Tudorache"'
Autor:
Cecilia Altuzarra, Altynshash Jaxybayeva, Marta Gomez Garcia de la Banda, Bakhytkul Myrzaliyeva, Jon Andoni Urtizberea, Jean-Michel Vallat, Raluca Anca Tudorache, Meriem Tazir, Andoni Echaniz-Laguna, Alain Verloes, Susana Quijano-Roy, Bruno Francou
Publikováno v:
neurogenetics. 22:333-341
Congenital insensitivity to pain with anhidrosis (CIPA) is a rare autosomal recessive disease resulting from mutations in the NTRK1 gene encoding the neurotrophic tyrosine kinase-1 receptor. In this multicenter observational retrospective study, we i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aa20ee8bbda3184a88f30e5a12c6c645
https://doi.org/10.1007/s10048-021-00668-z
https://doi.org/10.1007/s10048-021-00668-z
Autor:
Andoni, Echaniz-Laguna, Cecilia, Altuzarra, Alain, Verloes, Marta Gomez Garcia, De La Banda, Susana, Quijano-Roy, Raluca Anca, Tudorache, Altynshash, Jaxybayeva, Bakhytkul, Myrzaliyeva, Meriem, Tazir, Jean-Michel, Vallat, Bruno, Francou, Jon Andoni, Urtizberea
Publikováno v:
Neurogenetics. 22(4)
Congenital insensitivity to pain with anhidrosis (CIPA) is a rare autosomal recessive disease resulting from mutations in the NTRK1 gene encoding the neurotrophic tyrosine kinase-1 receptor. In this multicenter observational retrospective study, we i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d56e759647366d34338ec8bba470ec74
https://pubmed.ncbi.nlm.nih.gov/34405299
https://pubmed.ncbi.nlm.nih.gov/34405299