Two siblings with triple A syndrome and novel mutation presenting as hereditary polyneuropathy.
about
Long-term clinical follow-up and molecular genetic findings in eight patients with triple A syndrome.Identification of AAAS gene mutation in Allgrove syndrome: A report of three cases.Phenotype-genotype spectrum of AAA syndrome from Western India and systematic review of literature.Clinical and genetic characterisation of a series of patients with triple A syndrome.Low bone mineral density for age/osteoporosis in triple A syndrome-an overlooked symptom of unexplained etiology.
P2860
Two siblings with triple A syndrome and novel mutation presenting as hereditary polyneuropathy.
description
2010 nî lūn-bûn
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2010年の論文
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2010年学术文章
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2010年学术文章
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2010年学术文章
@zh-cn
2010年学术文章
@zh-hans
2010年学术文章
@zh-my
2010年学术文章
@zh-sg
2010年學術文章
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2010年學術文章
@zh-hant
name
Two siblings with triple A syn ...... as hereditary polyneuropathy.
@en
Two siblings with triple A syn ...... as hereditary polyneuropathy.
@nl
type
label
Two siblings with triple A syn ...... as hereditary polyneuropathy.
@en
Two siblings with triple A syn ...... as hereditary polyneuropathy.
@nl
prefLabel
Two siblings with triple A syn ...... as hereditary polyneuropathy.
@en
Two siblings with triple A syn ...... as hereditary polyneuropathy.
@nl
P2093
P2860
P1476
Two siblings with triple A syn ...... as hereditary polyneuropathy.
@en
P2093
Andrija Stanimirović
Angela Huebner
Katrin Koehler
Miroslav Dumić
Nataša Rojnić-Putarek
Nina Barišić
Vesna Kušec
P2860
P2888
P304
P356
10.1007/S00431-010-1314-4
P577
2010-10-08T00:00:00Z