INTERGEN Genetics and Rare Diseases Diagnosis Research & Application Center
Industry / private company
Location:
Ankara,
Turkey (TR)
ISNI: 000000047553324X
ROR: https://ror.org/04fpsr797
Show on Map:
Episodic psychosis, ataxia, motor neuropathy with pyramidal signs (PAMP sydrome) caused by a novel mutation in ADPRHL2 (AHR3) (2021)
Durmus H, Mertoğlu E, Sticht H, Ceylaner S, Kulaksızoğlu IB, Hashemolhosseini S, Uçar EÖ, Parman Y
Journal article
EPISODIC PSYCHOSIS, ATAXIA, MOTOR NEUROPATHY CAUSED BY A NOVEL MUTATION IN ADPRHL2 (2020)
Durmus H, Sticht H, Ceylaner S, Hashemolhosseini S, Parmn Y
Conference contribution
Rare slow channel congenital myasthenic syndromes without repetitive compound muscle action potential and dramatic response to low dose fluoxetine (2020)
Durmus H, Sticht H, Ceylaner S, Hashemolhosseini S, Deymeer F
Journal article