ANALYSIS OF THE MOLECULAR MECHANISMS LEADING TO THE INACTIVATION OF THE RECEPTOR TYROSINE KINASES RET AND NTRK1 IN HSCR AND CIPA CONGENITAL DISORDERS

2 Anni 1997/1999
72.304€ Totale Fondi

Descrizione non disponibile

Pubblicazioni Scientifiche

1999-04-01 AMERICAN JOURNAL OF HUMAN GENETICS
A novel NTRK1 mutation associated with congenital insensitivity to pain with anhidrosis
2000-01-01 JOURNAL OF CELLULAR PHYSIOLOGY
The Gly571arg mutation, associated with the autonomic and sensory disorder congenital insensitivity to pain with anhidrosis, causes the inactivation of the NTRK1/nerve growth factor receptor

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