Acid ceramidase deficiency due to mutations in ASAH1, presenting asFarber Disease: Diagnostic data from the first-ever natural history study
Author
Torcoletti, Marta
ÖZEN, SEZA
Batu, Ezgi Deniz
Kimura, Alan
Harmatz, Paul
GÖKÇAY, GÜLDEN FATMA
solyom, Alexander
Ferreira, Carlos R
Mitchell, John
Guelbert, Norberto
ÖNENLİ MUNGAN, HALİSE NESLİHAN
BULUT, FATMA DERYA
Magnusson, Bo
Sundberg, Erik
Lampe, Christina
Arslan, Nur
MAKAY, BALAHAN
Puri, Ratna
Bijarnia Makay, Sunita
Selim, Laila
Gamal el Din, I
Kapoor, Seema
DiRocco, Maja
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