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Rat neurological disease creeping is caused by a mutation in the reelin gene

✍ Scribed by Norihide Yokoi; Misako Namae; He-Yao Wang; Ken Kojima; Masanori Fuse; Kazuki Yasuda; Tadao Serikawa; Susumu Seino; Kajuro Komeda


Book ID
117386107
Publisher
Elsevier Science
Year
2003
Tongue
English
Weight
694 KB
Volume
112
Category
Article
ISSN
0169-328X

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ABCD syndrome is caused by a homozygous
✍ Verheij, Joke B.G.M. ;Kunze, JοΏ½rgen ;Osinga, Jan ;van Essen, Anthonie J. ;Hofstr πŸ“‚ Article πŸ“… 2002 πŸ› John Wiley and Sons 🌐 English βš– 106 KB πŸ‘ 2 views

## Abstract ABCD syndrome is an autosomal recessive syndrome characterized by albinism, black lock, cell migration disorder of the neurocytes of the gut (Hirschsprung disease [HSCR]), and deafness. This phenotype clearly overlaps with the features of the Shah‐Waardenburg syndrome, comprising sensor