Atypical forms of Rett syndrome

scientific article published in January 1986

Atypical forms of Rett syndrome is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1002/AJMG.1320250521
P698PubMed publication ID3087180

P2093author name stringAicardi J
Goutières F
P921main subjectRett syndromeQ917357
P304page(s)183-194
P577publication date1986-01-01
P1433published inAmerican journal of medical genetics. SupplementQ27709574
P1476titleAtypical forms of Rett syndrome
P478volume1

Reverse relations

cites work (P2860)
Q35447640CDKL5/STK9 is mutated in Rett syndrome variant with infantile spasms
Q38375116Clinical and biological progress over 50 years in Rett syndrome.
Q28260149Clinical and electroencephalographic features in patients with CDKL5 mutations: two new Italian cases and review of the literature
Q34296510Is Rett syndrome a subtype of pervasive developmental disorders?
Q70282089Multi-institutional survey of the Rett syndrome in Japan
Q24534159Mutations in the X-linked cyclin-dependent kinase-like 5 (CDKL5/STK9) gene are associated with severe neurodevelopmental retardation
Q24644799NTNG1 mutations are a rare cause of Rett syndrome
Q48242577New experience with Rett syndrome in France: the problem of atypical cases
Q33677688Rett syndrome
Q24616417Rett syndrome and MeCP2: linking epigenetics and neuronal function
Q24596295Rett syndrome: revised diagnostic criteria and nomenclature
Q36922496The association between behavior and genotype in Rett syndrome using the Australian Rett Syndrome Database.
Q36443010The relationship of Rett syndrome and MECP2 disorders to autism.
Q41920459Widened clinical spectrum of the Q128P MECP2 mutation in Rett syndrome

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