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D. Hendig
D. Hendig
Ruhr University Bochum
Exome sequencing
Missense mutation
Genetics
Phenotype
XYLT2
1
Papers
11
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Homozygous XYLT2 variants as a cause of spondyloocular syndrome
2018
Clinical Genetics
Muhammad Umair
Gertrud Eckstein
G. Rudolph
T. M. Strom
Elisabeth Graf
D. Hendig
J. Hoover
J. Alanay
Thomas Meitinger
Heinrich Schmidt
Wasim Ahmad
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Citations (11)
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