Open AccessEIF2S3 Mutations Associated with Severe X-Linked Intellectual Disability Syndrome MEHMO
Author(s) -
Martina Škopková,
Friederike Hennig,
Shin Bs,
Turner Ce,
Daniela Staníková,
Katarína Brennerová,
Juraj Staník,
Utz Fischer,
Lyndal Henden,
U Müller,
Daniela Steinberger,
Esther LeshinskySilver,
Armand Bottani,
Tímea Kurdiová,
Jozef Ukropec,
Olga Nyitrayova,
Miriam Kolníková,
I Klimeś,
Guntram Borck,
Melanie Bahlo,
Haas Sa,
Kim JR,
Lotspeich-Cole LE,
Daniela Gašperíková,
TE Dever,
VM Kalscheuer
Publication year - 2018
Publication title -
yearbook of pediatric endocrinology
Language(s) - Uncategorized
Resource type - Journals
eISSN - 1662-4009
pISSN - 1662-3991
DOI - 10.1530/ey.15.2.9
Subject(s) - intellectual disability , genetics , medicine , biology
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