Recognizable phenotype with common occurrence of microcephal…
Recognizable phenotype with common occurrence of microcephaly%2C psychomotor retardation%2C but no spontaneous bone fractures in autosomal recessive cutis laxa type IIB due to PYCR1 mutations
Article, Chapter
Authors:
D. Kouwenberg
Publication:
Volume:155A,
Issue:9,
Page(s):2331-2332%3B author reply 2333-2334
Published:
2011
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