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Ma, D.-L
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Ma, D.-L
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Two novel SASH1 mutations in Chinese families with dyschromatosis universalis hereditaria
by
Habulieti, X.
,
Liu, J.-W
,
Ma
,
D
.-
L
,
Wang, R.-R
,
Zhang, X.
Published 2021
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Related Subjects
Adult
Article
Asian
Asians
China
Chinese
Female
Humans
Infant
Male
Mutation
Pedigree
Pigmentation Disorders
Prognosis
SASH1
SASH1 gene
SASH1 protein, human
SLY domain
Sanger sequencing
Skin Diseases, Genetic
Tumor Suppressor Proteins
adult
bioinformatics
case report
clinical feature
controlled study
dyschromatosis universalis hereditaria
familial disease
female
frameshift mutation
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